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Non-Neoplastic Disorder

MedGen UID:: 311052
•Concept ID:: C1709246
•: Disease or Syndrome

Synonym:

Non-Neoplastic Disease

Definition

Any disorder other than abnormal tissue growth resulting from uncontrolled cell proliferation. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVNon-Neoplastic Disorder

Pathological Conditions, Signs and Symptoms
- Pathological process
  - Disease
    - Non-Neoplastic Disorder
      - Non-Neoplastic Disorder by Site
        Non-Neoplastic Breast Disorder
        Atypical Vascular Lesion of Breast
        Breast adenosis
        Breast fibrocystic disease
        Breast Hamartoma
        Breast hypertrophy
        Breast hypoplasia
        Fat necrosis of breast
        Gynecomastia
        Lactation disease
        Lactocele
        Mammary duct ectasia
        Mastitis
        Non-Neoplastic Cardiovascular Disorder
        Arteriosclerotic Cardiovascular Disease
        Cardiac arrhythmia
        Congenital anomaly of cardiovascular system
        Non-Neoplastic Heart Disorder
        Non-Neoplastic Vascular Disorder
        Pulmonary artery stenosis
        Non-Neoplastic Connective and Soft Tissue Disorder
        Arthropathy
        Juvenile hyaline fibromatosis
        Non-Neoplastic Musculoskeletal Disorder
        Non-Neoplastic Soft Tissue Disorder
        Non-Neoplastic Digestive System Disorder
        Congenital Digestive System Disorder
        Infectious disease of digestive tract
        Non-Neoplastic Anal Disorder
        Non-Neoplastic Appendix Disorder
        Non-Neoplastic Esophageal Disorder
        Non-Neoplastic Hepatobiliary Disorder
        Non-Neoplastic Intestinal Disorder
        Non-Neoplastic Pancreatic Disorder
        Non-Neoplastic Stomach Disorder
        Peptic ulcer
        Non-Neoplastic Endocrine Disorder
        11-Beta-Hydroxylase Deficiency
        17-Alpha-Hydroxylase/17,20 Lyase Deficiency
        21-Hydroxylase Deficiency
        3 beta-Hydroxysteroid dehydrogenase deficiency
        Adrenal cortical hypofunction
        Atrophy of thyroid
        Autoimmune polyendocrinopathy
        Congenital Adrenal Gland Disorder
        Congenital Thyroid Gland Disorder
        Diabetes insipidus
        Disorder of AMH
        Disorder of AMH Receptor
        Disorder of Androgen Synthesis
        Endocrine Disorder Arising from Mental Factor
        Glucose metabolism disease
        Goiter
        Gonadal agenesis
        Hyperandrogenism due to cortisone reductase deficiency
        Hyperthyroidism
        Hypogonadism
        Hypoparathyroidism
        Hypopituitarism
        Hypothyroidism
        Mullerian aplasia and hyperandrogenism
        Pituitary gland hypoplasia
        Pseudohypoparathyroidism
        Pyknodysostosis
        Testosterone 17-beta-dehydrogenase deficiency
        Thyroiditis
        Turner syndrome
        Non-Neoplastic Eye Disorder
        Amaurosis fugax
        Blepharitis
        Blepharoconjunctivitis
        Cataract
        Choroideremia
        Congenital anomaly of eye
        Congenital ocular coloboma
        Contact lens overwear syndrome
        Cyclitis
        Disorder of eye due to diabetes mellitus
        Dry eye syndrome
        Eye infectious disease
        Fat Adherence Syndrome
        Glaucoma
        Hyphema
        Intraocular Lens Dislocation
        Iritis
        Keratoconjunctivitis
        Lens luxation
        Non-Neoplastic Conjunctival Disorder
        Non-Neoplastic Corneal Disorder
        Non-Neoplastic Eyelid Disorder
        Non-Neoplastic Lacrimal System Disorder
        Non-Neoplastic Retinal Disorder
        Non-Neoplastic Uveal Disorder
        Ocular melanocytosis
        Ocular vascular disorder
        Optic atrophy
        Ornithine aminotransferase deficiency
        Pars planitis
        Sunset Syndrome
        Uveitis-glaucoma-hyphema syndrome
        Vitreous detachment
        Non-Neoplastic Genitourinary System Disorder
        Genitourinary syndrome of menopause
        Infectious disease of genitourinary system
        Non-Neoplastic Reproductive System Disorder
        Non-Neoplastic Urinary System Disorder
        Non-Neoplastic Head and Neck Disorder
        Cholesteatoma
        Lymphedema of the Head and Neck
        Non-Neoplastic Ear Disorder
        Non-Neoplastic Neck Disorder
        Non-Neoplastic Oral Disorder
        Non-Neoplastic Salivary Gland Disorder
        Non-Neoplastic Sinonasal Disorder
        Non-Neoplastic Hematologic and Lymphocytic Disorder
        Abnormality of the coagulation cascade
        Amegakaryocytosis
        Anemia
        Benign Lymphoproliferative Disorder
        Congenital hematological disorder
        Cyclical neutropenia
        Evans syndrome
        Functional disorder of polymorphonuclear neutrophil
        Inherited bleeding disorder, platelet-type
        Methemoglobinemia
        Neonatal Leukopenia
        Paroxysmal nocturnal hemoglobinuria
        Pure red-cell aplasia
        Sinus histiocytosis with massive lymphadenopathy
        Spherocytosis
        Non-Neoplastic Nervous System Disorder
        Abnormality of the nervous system
        Autoimmune disorder of the nervous system
        Demyelinating disease
        Giant axonal neuropathy
        Infectious disease of the nervous system
        Leukodystrophy
        Myelitis
        Nerve palsy
        Neuronal intranuclear inclusion disease
        Non-Neoplastic Central Nervous System Disorder
        Non-Neoplastic Optic Nerve Disorder
        Non-Neoplastic Peripheral Nervous System Disorder
        Non-Neoplastic Trigeminal Nerve Disorder
        Non-Neoplastic Peritoneal and Retroperitoneal Disorder
        Non-Neoplastic Peritoneal Disorder
        Non-Neoplastic Retroperitoneal Disorder
        Non-Neoplastic Respiratory System Disorder
        Congenital malformation of the respiratory system
        Congenital tracheobronchomegaly
        Neonatal respiratory system disorder
        Non-Neoplastic Chronic Respiratory System Disorder
        Non-Neoplastic Lung Disorder
        Non-Neoplastic Tracheal Disorder
        Postprocedural respiratory disorders
        Sleep-Disordered Breathing
        Tracheobronchomalacia
        Non-Neoplastic Skin Disorder
        Acrokeratosis verruciformis of Hopf
        Anetoderma
        Atypical Vascular Lesion
        Bacterial infection of skin
        Bullous pemphigoid
        Chronic bullous dermatosis of childhood
        Chronic Cutaneous Graft Versus Host Disease
        Cutaneous abscess
        Cutaneous Rosai-Dorfman Disease
        Cutis laxa
        Dermal atrophy
        Epidermolysis bullosa
        Erythema multiforme
        Erythroderma
        Erythrokeratodermia variabilis
        Fox-Fordyce disease
        Generalized Cutaneous Reticulohistiocytosis
        Granuloma annulare
        Hamartoma of skin appendage
        Ichthyosis
        Keratoderma
        Keratosis pilaris
        Lentigo
        Lymphocytoma cutis
        Necrobiosis lipoidica
        Neonatal toxic erythema
        Non-Neoplastic Hair Disorder
        Non-neoplastic nevus
        Parana hard-skin syndrome
        Pemphigus
        Pityriasis lichenoides
        Pityriasis rubra pilaris
        Pityriasis versicolor
        Poikiloderma
        Pruritus
        Reactive cutaneous fibrous lesion
        Scleromyxedema
        Skin disorder
        Skin Disorder Arising from Mental Factor
        Skin infection
        Skin pigmentation disorder
        Skin sarcoidosis
        Skin tags
        Solar lentigo
        Solitary Cutaneous Reticulohistiocytosis
        Staphylococcal scalded skin syndrome
        Stevens-Johnson syndrome
        Toxic epidermal necrolysis
        Verruciform xanthoma
        Xanthelasma
        Xeroderma
        Non-Neoplastic Thoracic Disorder
        Non-Neoplastic Axillary Disorder
        Non-Neoplastic Chest Wall Disorder
        Non-Neoplastic Mediastinal Disorder
        Non-Neoplastic Pleural Disorder
        Non-Neoplastic Thymus Disorder
        Non-Neoplastic Vision Disorder
        Amblyopia
        Ametropia
        Binocular vision disease
        Blindness
        Reduced vision
        Strabismus
        Visual agnosia
      - Non-Neoplastic Disorder by Special Category
        Deformity
        Abnormality of Ventricle
        Cheiromegaly
        Collapsed Lumen
        Deformity of Forearm
        Diaphragmatic eventration
        Disfigurement
        Diverticulum
        Evagination
        Fetal anomaly
        Hallux valgus
        Hernia
        Heterotaxy
        Ingrown nail
        Megalencephaly
        Mucocele of salivary gland
        Musculoskeletal Deformity
        Nipple deformity
        Nose Deformity
        Pes planus
        Prolapse
        Ptosis
        Sinus
        Stenosis
        Supernumerary ribs
        Tissue or Organ Disruption
        Degenerative disorder
        Degenerative disease of the central nervous system
        Plexopathy
        Spinal Degenerative Disorder
        Endemic disease
        Hamartoma
        Benign Triton Tumor
        Central Nervous System Hamartoma
        Chondroid hamartoma
        Congenital hamartoma
        Connective tissue nevi
        Cowden syndrome
        Cutaneous hamartoma
        Cutaneous Neurocristic Hamartoma
        Ecchordosis physaliphora
        Fibrous hamartoma
        Hamartoma of Mature Cardiac Myocytes
        Hamartoma of the orbital region
        Hamartomatous polyp
        Hamartomatous polyposis
        Hyperpigmentation, progressive cribriform and zosteriform
        Linear nevus sebaceous syndrome
        Liver hamartoma
        Meningothelial Hamartoma
        Mesenchymal hamartoma
        Nasal hamartoma
        Odontoma
        Pallister-Hall syndrome
        Pancreatic hamartoma
        Renal hamartoma
        Retinal hamartoma
        Sinonasal Respiratory Epithelial Adenomatoid Hamartoma
        Sinonasal Seromucinous Hamartoma
        Spleen hamartoma
        Tuberous sclerosis syndrome
        Urinary bladder hamartoma
        Vascular hamartoma
        Hyperplasia
        Adenomatous Hyperplasia of the Ciliary Body
        Adrenal hyperplasia
        Atypical hyperplasia
        Basal cell hyperplasia
        Benign prostatic hyperplasia
        Bone marrow hyperplasia
        Breast Hyperplasia
        Cervical Mesonephric Remnants and Hyperplasia
        Circumferential Endothelial Hyperplasia
        Conjunctival Reactive Epithelial Hyperplasia
        Diffuse hyperplasia
        Drug-induced gingival hyperplasia
        Epithelial hyperplasia of skin
        Focal epithelial hyperplasia
        Foveolar hyperplasia
        Glandular hyperplasia
        Intercalated Duct Hyperplasia
        Intraductal hyperplasia
        Intraepithelial Melanocytic Hyperplasia
        Islet Glucagon Cell Hyperplasia
        Lymphoid hyperplasia
        Mesonephric Hyperplasia
        Mesothelial hyperplasia
        Multifocal nodular oncocytic hyperplasia of salivary gland
        Neuroendocrine cell hyperplasia of infancy
        Ovarian Leydig Cell Hyperplasia
        Parathyroid hyperplasia
        Pituitary Hyperplasia
        Reactive Epithelial Hyperplasia of the Ciliary Body
        Reactive Hyperplasia of the Retinal Pigment Epithelium
        Reserve Cell Hyperplasia
        Reticuloendotheliosis, X-linked
        Sebaceous hyperplasia
        Squamous Hyperplasia
        Stromal hyperplasia
        Thyroid C cell hyperplasia
        Urothelial hyperplasia
        Inflammatory disease
        Catheter-Related Inflammation
        Infectious disease
        Inflammatory bowel disease
        Inflammatory spondylopathy
        KSHV inflammatory cytokine syndrome
        Mastoiditis
        Mucositis
        Metabolic disease
        5,10-Methylenetetrahydrofolate reductase deficiency
        Abnormal blood ion concentration
        Abnormality of acid-base homeostasis
        Bronze diabetes
        Carbohydrate metabolism disease
        Carnosinemia
        Combined oxidative phosphorylation defect type 8
        Combined oxidative phosphorylation deficiency 33
        Dihydropyrimidine dehydrogenase deficiency
        disorder of calcium metabolism
        Disturbance of Temperature Regulation
        DNA Repair-Deficiency Disorders
        Emaciated
        Gout
        Hepatic methionine adenosyltransferase deficiency
        Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
        High density lipoprotein cholesterol level quantitative trait locus 6
        Hyperlactatemia
        Hyperlipoproteinemia
        Hyperlysinemia
        Hyperpipecolatemia
        Hypoalphalipoproteinemia
        Hypophosphatasia
        Imbalances, Water-Electrolyte
        Inborn errors of metabolism
        Inherited lipid metabolism disorder
        Iron metabolism disease
        Lipodystrophy
        Malabsorption syndrome
        Metabolic bone disorder
        Metabolic encephalopathy
        Mitochondrial disease
        Mitochondrial Enzyme Deficiency
        Nickel Metabolic Disorder
        Nutritional disorder
        Phosphorus metabolism disease
        polysyndactyly
        Porphyria
        Proteostasis deficiencies
        Skin Diseases, Metabolic
        Wasting disease
        Zinc deficiency
        Non-Communicable Disorder
        Radiation-Related Non-Neoplastic Disorder
        Mucositis following radiation therapy
        Radiation Anemia
        Radiation enteritis of intestine
        Radiation Sickness Syndrome
        Radiation-induced fibrous mediastinitis
        Radiation-induced xerostomia
        Rare Non-Neoplastic Disorder
        11q partial monosomy syndrome
        17q21 Microdeletion Syndrome
        22q Telomere Deletion Syndrome
        3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency
        Abetalipoproteinaemia
        Acatalasia
        Achard syndrome
        Achenbach syndrome
        Achondrogenesis
        Achromatopsia
        Acrocallosal syndrome
        Acrocephalosyndactyly
        Acrodermatitis
        Acrodysostosis 1
        Acromegaly
        Acromesomelic Dysplasia, PRKG2 Type
        Acute febrile neutrophilic dermatosis
        Acute intermittent porphyria
        Acyl-CoA oxidase deficiency
        Adenine phosphoribosyltransferase deficiency
        ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder
        Agnosia
        Aicardi syndrome
        Ainhum
        Albinism
        Alkaptonuria
        Allan-Herndon-Dudley syndrome
        Alpha thalassemia-X-linked intellectual disability syndrome
        Alpha-methylacyl-CoA racemase deficiency
        Alstrom syndrome
        Analbuminemia
        Anaphylotoxin inactivator deficiency
        Andersen Tawil syndrome
        Anencephaly
        Angioosteohypertrophic syndrome
        Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
        Anti-glomerular basement membrane disease
        Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis
        Aprosencephaly
        Arginase deficiency
        Argininosuccinate lyase deficiency
        Arrhythmogenic right ventricular cardiomyopathy
        Arterial calcification, generalized, of infancy, 1
        Arthrogryposis
        Ataxia-telangiectasia-like disorder 1
        Atransferrinemia
        Atrophia bulborum hereditaria
        Atrophic muscular disease
        Auditory processing disorder
        Autosomal dominant deafness - onychodystrophy syndrome
        Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
        Autosomal recessive DOPA responsive dystonia
        Autosomal recessive hypohidrotic ectodermal dysplasia syndrome
        Autosomal recessive nonsyndromic hearing loss 4
        Autosomal recessive nonsyndromic hearing loss 28
        Autosomal recessive nonsyndromic hearing loss 39
        Autosomal recessive nonsyndromic hearing loss 49
        Axenfeld-Rieger syndrome type 1
        Azorean disease
        Bartter syndrome
        Beaded hair
        Beare-Stevenson cutis gyrata syndrome
        Benign intracranial hypertension
        Bernard Soulier syndrome
        Beta-Methylcrotonylglycinuria
        Bifunctional peroxisomal enzyme deficiency
        Bilirubin encephalopathy
        Biotinidase deficiency
        Borjeson-Forssman-Lehmann syndrome
        Brown-Séquard syndrome
        Calciphylaxis
        Camptomelic dysplasia
        Cancrum oris
        Carbonic anhydrase I deficiency
        Cardio-facio-cutaneous syndrome
        Carnitine acylcarnitine translocase deficiency
        Carnitine palmitoyl transferase 1A deficiency
        Carnitine palmitoyltransferase II deficiency
        Caroli disease
        Cat eye syndrome
        Cataplexy
        Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
        Cerebral cysticercosis
        Channelopathy-associated congenital insensitivity to pain, autosomal recessive
        CHARGE association
        Chiari malformation
        Chilblains
        Cholestanol storage disease
        Cholestasis-edema syndrome, Norwegian type
        Chondrodysplasia punctata
        Chorea
        Chorea-acanthocytosis
        Chromosome 1p36 deletion syndrome
        Chromosome 2q37 deletion syndrome
        Cleidocranial dysostosis
        Coarctation of aorta
        CODAS syndrome
        Coenzyme Q10 deficiency
        Coffin-Lowry syndrome
        COFS syndrome
        Cogan-Reese syndrome
        Combined molybdoflavoprotein enzyme deficiency
        Complex regional pain syndrome type 1
        Complex regional pain syndrome type 2
        Congenital amegakaryocytic thrombocytopenia
        Congenital aniridia
        Congenital bilateral aplasia of vas deferens from CFTR mutation
        Congenital defect of folate absorption
        Congenital disorder of deglycosylation
        Congenital disorder of glycosylation
        Congenital dyserythropoietic anemia
        Congenital generalized lipodystrophy
        Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
        Congenital multicore myopathy with external ophthalmoplegia
        Congenital myasthenic syndrome
        Congenital myopathy with fiber type disproportion
        Congenital pseudoarthrosis of the tibia
        Congenital sensory neuropathy with selective loss of small myelinated fibers
        Congenital structural myopathy
        Constriction ring syndrome
        Cortical Dysplasia-Focal Epilepsy Syndrome
        Cranioectodermal dysplasia
        Craniofacial microsomia
        Craniosynostosis syndrome
        Crouzon syndrome
        Cryopyrin associated periodic syndrome
        Cryptophthalmos syndrome
        Crystal-Storing Histiocytosis
        Cutaneous porphyria
        Cystathioninuria
        Cystinuria
        Cytochrome-c oxidase deficiency
        D-Glyceric aciduria
        Dandy-Walker syndrome
        De Lange syndrome
        DE SANCTIS-CACCHIONE SYNDROME
        Deafness due to Connexin 26 Gene Anomaly
        Deficiency of aromatic-L-amino-acid decarboxylase
        Deficiency of butyryl-CoA dehydrogenase
        Deficiency of hydroxymethylglutaryl-CoA lyase
        Deficiency of isobutyryl-CoA dehydrogenase
        Deficiency of mevalonate kinase
        Deletion of long arm of chromosome 18
        Deletion of short arm of chromosome 18
        Dentatorubral-pallidoluysian atrophy
        Dentinogenesis imperfecta
        Dextrocardia
        Diaphyseal dysplasia
        Diastrophic dysplasia
        Diffuse idiopathic skeletal hyperostosis
        Digital flexor tenosynovitis
        Disorder of the urea cycle metabolism
        DNA ligase IV deficiency
        Dominant hereditary optic atrophy
        Double Y syndrome
        Drug- and Toxin-Induced Pulmonary Arterial Hypertension
        Duane retraction syndrome
        Dubowitz syndrome
        Dyggve-Melchior-Clausen syndrome
        Ebstein anomaly
        Ectodermal dysplasia and immune deficiency
        Ectrodactyly
        Ectromelia
        Eiken Type Chondrodysplasia
        Ellis-van Creveld syndrome
        Empty sella syndrome
        Encephalocele
        Epilepsy, familial focal, with variable foci 1
        Erythromelalgia
        Erythropoietic protoporphyria
        Exstrophy-epispadias complex
        Factor V Leiden mutation
        Familial aplasia of the vermis
        Familial digital arthropathy-brachydactyly
        Familial dysautonomia
        Familial episodic pain syndrome with predominantly lower limb involvement
        Familial hypokalemia-hypomagnesemia
        Familial Mediterranean fever
        Familial partial lipodystrophy
        Familial periodic paralysis
        Farber lipogranulomatosis
        Fatal familial insomnia
        Feingold syndrome
        Felty syndrome
        Fetal akinesia deformation sequence 1
        Fibromuscular dysplasia
        Floating-Harbor syndrome
        Focal dermal hypoplasia
        Fragile X syndrome
        Friedreich ataxia
        Frontonasal dysplasia
        Frontotemporal dementia
        Fryns syndrome
        Fuchs endothelial dystrophy
        G6PD deficiency
        Galloway-Mowat syndrome
        Gastrointestinal defect and immunodeficiency syndrome
        Gastroschisis
        Genu varum
        Gerstmann-Straussler-Scheinker syndrome
        Glanzmann thrombasthenia
        Glucocorticoid deficiency with achalasia
        Glutaric aciduria, type 1
        Glycogen storage disease
        Granulomatosis with polyangiitis
        Gray platelet syndrome
        Griscelli syndrome type 2
        GTP cyclohydrolase I deficiency
        Gynatresia
        Hajdu-Cheney syndrome
        Hallermann-Streiff syndrome
        Hantavirus pulmonary syndrome
        HELLP syndrome
        Hemophagocytic lymphohistiocytosis
        Hemorrhagic fever-renal syndrome
        Hereditary acrodermatitis enteropathica
        Hereditary angioneurotic edema
        Hereditary antithrombin deficiency
        Hereditary coproporphyria
        Hereditary fructosuria
        Hereditary hemochromatosis
        Hereditary hyperbilirubinemia
        Hereditary insensitivity to pain with anhidrosis
        Hereditary orotic aciduria
        Hereditary persistence of fetal hemoglobin
        Hereditary sensory and autonomic neuropathy type 1
        Hereditary sensory and autonomic neuropathy type 7
        Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1
        Heritable pulmonary arterial hypertension
        Hermansky-Pudlak syndrome
        Herpes gestationis
        High molecular weight kininogen deficiency
        Holmes-Adie syndrome
        Holocarboxylase synthetase deficiency
        Holoprosencephaly sequence
        Holoprosencephaly-postaxial polydactyly syndrome
        Holt-Oram syndrome
        Homocystinuria
        Hutchinson-Gilford syndrome
        Hyaline Membrane Syndrome
        Hydroa vacciniforme
        Hydrops fetalis
        Hymenolepiasis
        Hyperammonemia, type III
        HyperCKmia
        Hyperkalemic periodic paralysis
        Hyperlipoproteinemia, type I
        Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
        Hypohidrotic X-linked ectodermal dysplasia
        Hypokalemic periodic paralysis
        Hypoparathyroidism-retardation-dysmorphism syndrome
        Hypoplastic enamel-onycholysis-hypohidrosis syndrome
        Idiopathic Basal Ganglia Calcification
        Idiopathic basal ganglia calcification 1
        Idiopathic CD4-positive T-lymphocytopenia
        Idiopathic hypersomnia
        IgAD1
        Immunodeficiency-centromeric instability-facial anomalies syndrome 1
        Imperforate anus
        Imperforate Vagina
        Inborn glycerol kinase deficiency
        Incontinentia pigmenti syndrome
        Infantile cortical hyperostosis
        Infantile neuroaxonal dystrophy
        Infection by larvae of Trichinella
        Infection by Paragonimus
        Inosine triphosphatase deficiency
        Intellectual disability, autosomal dominant 1
        Intellectual disability, autosomal dominant 39
        Intellectual disability, autosomal recessive 34
        Intellectual disability, X-linked 1
        Intestinal atresia
        Iridocorneal endothelial syndrome
        Isolated Pierre-Robin syndrome
        Jackson-Weiss syndrome
        Jervell and Lange-Nielsen syndrome
        Jeune thoracic dystrophy
        Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
        Kabuki syndrome
        Kearns-Sayre syndrome
        Kennedy disease
        Keratosis follicularis
        Kimura disease
        Kleefstra syndrome 1
        Kleine-Levin syndrome
        Klippel-Feil syndrome
        Kluver-Bucy syndrome
        Kniest dysplasia
        Lafora disease
        Landau-Kleffner syndrome
        Langer-Giedion syndrome
        Lateral medullary syndrome
        Leber congenital amaurosis
        Leber optic atrophy
        Legg-Calve-Perthes disease
        Leigh syndrome
        Lennox-Gastaut syndrome
        Leprechaunism syndrome
        Leprosy
        Leptospirosis
        Leri-Weill dyschondrosteosis
        Lesch-Nyhan syndrome
        Leukoencephalopathy with mild cerebellar ataxia and white matter edema
        Liddle syndrome
        Lipase deficiency, combined
        Lipid proteinosis
        Lipomatosis dolorosa
        Lissencephaly
        Loeys-Dietz syndrome
        Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
        Long chain acyl-CoA dehydrogenase deficiency
        Lowe syndrome
        Lysinuric protein intolerance
        Lysosomal storage disease
        Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
        Malakoplakia
        Malformation of cortical development
        Malignant atrophic papulosis
        Malignant hyperthermia of anesthesia
        Malignant migrating partial seizures of infancy
        Mallory-Weiss syndrome
        Mandibuloacral dysplasia with type A lipodystrophy
        Mansonelliasis
        Maple syrup urine disease
        Marburg virus disease
        Marfan syndrome
        Marshall syndrome
        MASA syndrome
        Mayer-Rokitansky-Kuster-Hauser syndrome
        Meckel-Gruber syndrome
        Medium-chain acyl-coenzyme A dehydrogenase deficiency
        Meesmann corneal dystrophy
        Megacystis, microcolon, hypoperistalsis syndrome
        Melkersson-Rosenthal syndrome
        Mendelian susceptibility to mycobacterial disease
        Menkes kinky-hair syndrome
        Mental Retardation, Autosomal Dominant 40
        Mental Retardation, X-linked 102
        MERRF syndrome
        Metaphyseal chondrodysplasia, Jansen type
        Metaphyseal chondrodysplasia, McKusick type
        Metatropic dysplasia
        Methylmalonic acidemia
        Microcephaly and chorioretinopathy 1
        Mitochondrial DNA depletion syndrome 12
        Mitochondrial DNA depletion syndrome 13
        Mitochondrial neurogastrointestinal encephalomyopathy
        Mitochondrial trifunctional protein deficiency
        Mitochondrially Inherited Nonsyndromic Sensorineural Deafness
        Mixed connective tissue disease
        Mosaic trisomy 14
        Mowat-Wilson syndrome
        Moyamoya disease
        Mucous membrane pemphigoid
        Muenke syndrome
        Mulibrey nanism syndrome
        Mullerian inhibiting factor deficiency
        Multicentric carpo-tarsal osteolysis with or without nephropathy
        Multicentric osteolysis nodulosis arthropathy spectrum
        Multiple acyl-CoA dehydrogenase deficiency
        Multiple system atrophy
        Muscular dystrophy
        Myhre syndrome
        Myokymia
        Myositis disease
        Myotonic syndrome
        NADH Dehydrogenase Deficiency
        Nail-patella syndrome
        Nelson Syndrome
        Neonatal pseudo-hydrocephalic progeroid syndrome
        Neonatal-onset encephalopathy with rigidity and seizures
        Nephrocalcinosis
        Nephrogenic fibrosing dermopathy
        Neural tube defect
        Neurodegeneration with brain iron accumulation 4
        Neurodegeneration with brain iron accumulation 5
        Neuromyelitis optica
        Neutral 1 amino acid transport defect
        Non-ketotic hyperglycinemia
        Non-Trisomic Autosomal Aneuploidy
        Noonan syndrome with multiple lentigines
        Norum disease
        Ochronosis disorder
        Olivopontocerebellar atrophy
        Optic neuropathy
        Orofacial cleft 1
        Orofaciodigital syndrome I
        Orofaciodigital syndrome type 6
        Oromandibular-limb hypogenesis spectrum
        Ossification of posterior longitudinal ligament
        Osteochondrodysplasia
        Osteopetrosis with renal tubular acidosis
        Osteopoikilosis
        Oto-palato-digital syndrome, type I
        Pachydermoperiostosis syndrome
        Pachyonychia congenita syndrome
        Pain agnosia
        Pallister-Killian syndrome
        Pancreatic triacylglycerol lipase deficiency
        Panuveitis
        Papillon-Lefèvre syndrome
        Paroxysmal extreme pain disorder
        Pearson syndrome
        Pelger-Huët anomaly
        Pelizaeus-Merzbacher disease
        Pentalogy of Cantrell
        Peritoneal Panniculitis
        Persistent fetal circulation syndrome
        Peters plus syndrome
        Pettigrew syndrome
        Phelan-McDermid syndrome
        Phosphoenolpyruvate carboxykinase (GTP) deficiency
        Pick disease
        Piebaldism
        Pigmentary pallidal degeneration
        PIK3CA related overgrowth syndrome
        PIK3R1 Deficiency
        Pinta disease
        Piriformis syndrome
        Plague
        Plasma Kallikrein Deficiency
        Platelet-type bleeding disorder 17
        Plummer-Vinson syndrome
        Poikiloderma with neutropenia
        Poland anomaly
        POLG-Related Spectrum Disorders
        Popliteal pterygium syndrome
        Porphobilinogen synthase deficiency
        Porphyria cutanea tarda
        Potocki-Lupski syndrome
        Potocki-Shaffer syndrome
        Prekallikrein deficiency
        Primary ciliary dyskinesia
        Primary familial hypertrophic cardiomyopathy
        Primary lateral sclerosis
        Primary progressive aphasia
        Progressive bulbar palsy
        Progressive muscular atrophy
        Progressive myositis ossificans
        Progressive supranuclear palsy
        Prolidase deficiency
        Prosopagnosia
        Proteus syndrome
        Prune belly syndrome
        Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
        Pseudoexfoliation glaucoma
        Pseudohermaphroditism
        Pseudohypoaldosteronism
        Pseudohypoparathyroidism type I A
        Pseudoxanthoma elasticum
        Pyruvate carboxylase deficiency
        Pyruvate dehydrogenase complex deficiency
        Radial aplasia-thrombocytopenia syndrome
        Relapsing polychondritis
        Renal carnitine transport defect
        Retinoschisis
        Rett syndrome
        Rhizomelic dysplasia
        Rippling muscle disease 2
        Roberts-SC phocomelia syndrome
        Robinow syndrome
        Russell-Silver syndrome
        SAPHO syndrome
        Schilder disease
        Schimke immuno-osseous dysplasia
        Schinzel-Giedion syndrome
        Scimitar syndrome
        Scleredema
        Sclerosteosis
        Sea-blue histiocyte syndrome
        Seckel syndrome
        Selective Antibody Deficiency with Normal Immunoglobulins
        Septo-optic dysplasia sequence
        Short rib-polydactyly syndrome
        Short Stature Homeobox Deficiency
        Shprintzen-Goldberg syndrome
        Sitosterolemia
        Situs inversus with levocardia
        Sjögren-Larsson syndrome
        Smith-Lemli-Opitz syndrome
        Smith-Magenis syndrome
        Sotos syndrome
        Spasmodic torticollis
        Spinal muscular atrophy
        Sponastrime dysplasia
        Spondyloepimetaphyseal dysplasia with multiple dislocations
        Spondyloperipheral dysplasia
        Stargardt disease
        STAT3-related early-onset multisystem autoimmune disease
        Status epilepticus
        Stickler syndrome
        Stiff skin syndrome
        Stiff-man syndrome
        Subacute sclerosing panencephalitis
        SUNCT syndrome
        Superior mesenteric artery syndrome
        Surfactant Protein Deficiency
        Swyer James Syndrome
        Symmetrical dyschromatosis of extremities
        Synpolydactyly
        Syringomyelia
        Takotsubo cardiomyopathy
        Tangier disease
        Tay-Sachs disease
        Tear film insufficiency
        Thanatophoric dysplasia
        Thoracic outlet syndrome
        Thrombocytopenia 2
        Thyroid dysgenesis
        Thyroid hormone resistance syndrome
        Tissue Kallikrein Deficiency
        Togaviridae infectious disease
        Tolosa-Hunt syndrome
        Transcobalamin II deficiency
        Transient global amnesia
        Transposition of the great arteries
        Treacher Collins syndrome
        Triatrial heart
        Trichorhinophalangeal dysplasia type I
        Trichothiodystrophy
        Triploidy
        True hermaphroditism
        Tuberculosis of meninges
        Uniparental disomy
        Usher syndrome
        Van der Woude syndrome
        Variegate porphyria
        Vascular ectasia of gastric antrum
        Very long chain acyl-CoA dehydrogenase deficiency
        Visceral heterotaxy
        Vitelliform macular dystrophy
        Vogt-Koyanagi-Harada disease
        Waardenburg syndrome
        Wandering spleen
        Waterhouse-Friderichsen Syndrome
        Weaver syndrome
        Weill-Marchesani syndrome
        Wernicke-Korsakoff syndrome
        West syndrome
        Whipple disease
        White sponge nevus
        Williams syndrome
        Wilson disease
        Winchester syndrome
        Wolfram syndrome
        X-linked intellectual disability Cabezas type
        Xeroderma pigmentosum-Cockayne syndrome complex
        XXXY and XXXXY Syndrome
        YARSopathy
        Yellow nail syndrome

Professional guidelines

PubMed

Pituitary stalk thickening: the role of an innovative MRI imaging analysis which may assist in determining clinical management.

Sbardella E, Joseph RN, Jafar-Mohammadi B, Isidori AM, Cudlip S, Grossman AB
Eur J Endocrinol 2016 Oct;175(4):255-63. Epub 2016 Jul 14 doi: 10.1530/EJE-16-0455. PMID: 27418059

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Recent clinical studies

Etiology

Ovarian Leydig Cell Tumor and Ovarian Hyperthecosis in a Postmenopausal Woman: A Case Report and Literature Review.

Bužinskienė D, Marčiukaitytė R, Šidlovska E, Rudaitis V
Medicina (Kaunas) 2023 Jun 6;59(6) doi: 10.3390/medicina59061097. PMID: 37374301 Free PMC Article

Pituitary stalk thickening: the role of an innovative MRI imaging analysis which may assist in determining clinical management.

Sbardella E, Joseph RN, Jafar-Mohammadi B, Isidori AM, Cudlip S, Grossman AB
Eur J Endocrinol 2016 Oct;175(4):255-63. Epub 2016 Jul 14 doi: 10.1530/EJE-16-0455. PMID: 27418059

Analysis of the factors related to the decision of restoring intestinal continuity after Hartmann's procedure.

Roque-Castellano C, Marchena-Gomez J, Hemmersbach-Miller M, Acosta-Merida A, Rodriguez-Mendez A, Fariña-Castro R, Hernandez-Romero J
Int J Colorectal Dis 2007 Sep;22(9):1091-6. Epub 2007 Jan 26 doi: 10.1007/s00384-007-0272-4. PMID: 17256137

Inappropriate secretion of thyroid-stimulating hormone.

Ann Intern Med 1981 Sep;95(3):339-51. doi: 10.7326/0003-4819-95-3-339. PMID: 7023312

See all (4)

Diagnosis

Ovarian Leydig Cell Tumor and Ovarian Hyperthecosis in a Postmenopausal Woman: A Case Report and Literature Review.

Bužinskienė D, Marčiukaitytė R, Šidlovska E, Rudaitis V
Medicina (Kaunas) 2023 Jun 6;59(6) doi: 10.3390/medicina59061097. PMID: 37374301 Free PMC Article

Sclerosing Mesenteritis.

Danford CJ, Lin SC, Wolf JL
Am J Gastroenterol 2019 Jun;114(6):867-873. doi: 10.14309/ajg.0000000000000167. PMID: 30829677

Pituitary stalk thickening: the role of an innovative MRI imaging analysis which may assist in determining clinical management.

Sbardella E, Joseph RN, Jafar-Mohammadi B, Isidori AM, Cudlip S, Grossman AB
Eur J Endocrinol 2016 Oct;175(4):255-63. Epub 2016 Jul 14 doi: 10.1530/EJE-16-0455. PMID: 27418059

Balloon catheter sialoplasty: a safety and feasibility pilot study.

Sionis S, Vedele A, Brennan PA, Fanni D, Puxeddu R
Br J Oral Maxillofac Surg 2013 Apr;51(3):228-30. Epub 2012 Jul 15 doi: 10.1016/j.bjoms.2012.06.011. PMID: 22795933

Foucar K, McKenna RW, Bloomfield CD, Bowers TK, Brunning RD
Cancer 1979 Apr;43(4):1285-96. doi: 10.1002/1097-0142(197904)43:4<1285::aid-cncr2820430416>3.0.co;2-j. PMID: 445330

See all (9)

Therapy

Myositis Ossificans Traumatica of the Medial Pterygoid Muscle After Third Molar Tooth Extraction: A Case Report and Review of Literature.

Karaali S, Emekli U
J Oral Maxillofac Surg 2018 Nov;76(11):2284.e1-2284.e5. Epub 2018 Jul 10 doi: 10.1016/j.joms.2018.06.174. PMID: 30076806

Analysis of the factors related to the decision of restoring intestinal continuity after Hartmann's procedure.

Chronic idiopathic thrombocytopenic purpura (ITP:) development of acute non-lymphocytic leukemia subsequent to treatment with cyclophosphamide.

Krause JR
Med Pediatr Oncol 1982;10(1):61-5. doi: 10.1002/mpo.2950100110. PMID: 7199614

Inappropriate secretion of thyroid-stimulating hormone.

Ann Intern Med 1981 Sep;95(3):339-51. doi: 10.7326/0003-4819-95-3-339. PMID: 7023312

Foucar K, McKenna RW, Bloomfield CD, Bowers TK, Brunning RD
Cancer 1979 Apr;43(4):1285-96. doi: 10.1002/1097-0142(197904)43:4<1285::aid-cncr2820430416>3.0.co;2-j. PMID: 445330

See all (5)

Prognosis

Ovarian Leydig Cell Tumor and Ovarian Hyperthecosis in a Postmenopausal Woman: A Case Report and Literature Review.

Bužinskienė D, Marčiukaitytė R, Šidlovska E, Rudaitis V
Medicina (Kaunas) 2023 Jun 6;59(6) doi: 10.3390/medicina59061097. PMID: 37374301 Free PMC Article

Sclerosing Mesenteritis.

Danford CJ, Lin SC, Wolf JL
Am J Gastroenterol 2019 Jun;114(6):867-873. doi: 10.14309/ajg.0000000000000167. PMID: 30829677

Pituitary stalk thickening: the role of an innovative MRI imaging analysis which may assist in determining clinical management.

Sbardella E, Joseph RN, Jafar-Mohammadi B, Isidori AM, Cudlip S, Grossman AB
Eur J Endocrinol 2016 Oct;175(4):255-63. Epub 2016 Jul 14 doi: 10.1530/EJE-16-0455. PMID: 27418059

Analysis of the factors related to the decision of restoring intestinal continuity after Hartmann's procedure.

Chronic idiopathic thrombocytopenic purpura (ITP:) development of acute non-lymphocytic leukemia subsequent to treatment with cyclophosphamide.

Krause JR
Med Pediatr Oncol 1982;10(1):61-5. doi: 10.1002/mpo.2950100110. PMID: 7199614

See all (5)

Clinical prediction guides

Pituitary stalk thickening: the role of an innovative MRI imaging analysis which may assist in determining clinical management.

Sbardella E, Joseph RN, Jafar-Mohammadi B, Isidori AM, Cudlip S, Grossman AB
Eur J Endocrinol 2016 Oct;175(4):255-63. Epub 2016 Jul 14 doi: 10.1530/EJE-16-0455. PMID: 27418059

Cranial fasciitis in an 8-year-old boy: clinical and histopathologic features.

Yébenes M, Gilaberte M, Romaní J, Lloreta J, Pujol RM
Pediatr Dermatol 2007 Jul-Aug;24(4):E26-30. doi: 10.1111/j.1525-1470.2007.00434.x. PMID: 17845151

Analysis of the factors related to the decision of restoring intestinal continuity after Hartmann's procedure.

Massive papillary dermal fatty infiltration in a patient with psoriasis.

Lee J, Bhawan J, Rothman K
J Cutan Pathol 1995 Apr;22(2):182-4. doi: 10.1111/j.1600-0560.1995.tb01405.x. PMID: 7560355

See all (4)

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Recent clinical studies

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Clinical prediction guides

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