Congenital Abnormalities

Malformations of organs or body parts during development in utero.

Year introduced: 2008 (1963)

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Subheadings:

Restrict to MeSH Major Topic.

Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C16.131

MeSH Unique ID: D000013

Entry Terms:

• Abnormality, Congenital
• Congenital Abnormality
• Deformities
• Deformity
• Congenital Defects
• Congenital Defect
• Defect, Congenital
• Defects, Congenital
• Abnormalities, Congenital
• Birth Defects
• Birth Defect
• Defect, Birth
• Fetal Malformations
• Fetal Malformation
• Malformation, Fetal
• Fetal Anomalies
• Anomaly, Fetal
• Fetal Anomaly

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Drug-Induced
Abnormalities, Multiple
22q11 Deletion Syndrome +
Alagille Syndrome
Angelman Syndrome
Barth Syndrome
Basal Cell Nevus Syndrome
Beckwith-Wiedemann Syndrome
Bloom Syndrome
Branchio-Oto-Renal Syndrome
Carney Complex
Ciliopathies +
Cockayne Syndrome
Costello Syndrome
Cri-du-Chat Syndrome
De Lange Syndrome
Deaf-Blind Disorders +
Donohue Syndrome
Down Syndrome
Ectodermal Dysplasia +
Fraser Syndrome
Gardner Syndrome
Heterotaxy Syndrome
Holoprosencephaly
Incontinentia Pigmenti
Isolated Noncompaction of the Ventricular Myocardium
Laurence-Moon Syndrome
LEOPARD Syndrome
Loeys-Dietz Syndrome
Marfan Syndrome
Mobius Syndrome
Monilethrix
Nail-Patella Syndrome
Netherton Syndrome
Nevus, Sebaceous of Jadassohn
Oculocerebrorenal Syndrome
Orofaciodigital Syndromes
Pallister-Hall Syndrome
Pentalogy of Cantrell
POEMS Syndrome
Polycystic Kidney Diseases +
Prader-Willi Syndrome
Prolidase Deficiency
Proteus Syndrome
Prune Belly Syndrome
Rubella Syndrome, Congenital
Rubinstein-Taybi Syndrome
Short Rib-Polydactyly Syndrome
Silver-Russell Syndrome
Smith-Lemli-Opitz Syndrome
Smith-Magenis Syndrome
Sotos Syndrome
Trichothiodystrophy Syndromes
Trisomy 13 Syndrome
Trisomy 18 Syndrome
Waardenburg Syndrome
Weill-Marchesani Syndrome
Wolf-Hirschhorn Syndrome
Zellweger Syndrome
Abnormalities, Radiation-Induced
Abnormalities, Severe Teratoid
Anencephaly
Twins, Conjoined
Aicardi Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital +
Vascular Malformations +
Chromosome Disorders
22q11 Deletion Syndrome +
Angelman Syndrome
Beckwith-Wiedemann Syndrome
Branchio-Oto-Renal Syndrome
Cri-du-Chat Syndrome
De Lange Syndrome
Down Syndrome
Holoprosencephaly
Jacobsen Distal 11q Deletion Syndrome
Prader-Willi Syndrome
Rubinstein-Taybi Syndrome
Sex Chromosome Disorders +
Silver-Russell Syndrome
Smith-Magenis Syndrome
Sotos Syndrome
Trisomy 13 Syndrome
Trisomy 18 Syndrome
WAGR Syndrome
Williams Syndrome
Wolf-Hirschhorn Syndrome
Congenital Microtia
Digestive System Abnormalities
Anorectal Malformations
Anus, Imperforate
Biliary Atresia
Choledochal Cyst +
Diaphragmatic Eventration
Esophageal Atresia
Hirschsprung Disease
Intestinal Atresia
Meckel Diverticulum
Pancreas Divisum
Pancreaticobiliary Maljunction
Eye Abnormalities
Aniridia +
Anophthalmos
Blepharophimosis
Coloboma
Ectopia Lentis
Familial Exudative Vitreoretinopathies
Fraser Syndrome
Hydrophthalmos
Microphthalmos
Persistent Hyperplastic Primary Vitreous
Retinal Dysplasia
Hernias, Diaphragmatic, Congenital
Lymphatic Abnormalities
22q11 Deletion Syndrome +
Lymphangiectasis, Intestinal
Musculoskeletal Abnormalities
Arthrogryposis
Campomelic Dysplasia
Cervical Rib Syndrome
Craniofacial Abnormalities +
Developmental Dysplasia of the Hip +
Funnel Chest
Gastroschisis
Hajdu-Cheney Syndrome
Hip Dislocation, Congenital
Klippel-Feil Syndrome
Laryngomalacia
Limb Deformities, Congenital +
Pectus Carinatum
Synostosis +
Tracheobronchomalacia +
Nervous System Malformations
Agenesis of Corpus Callosum +
Central Nervous System Cysts +
Central Nervous System Vascular Malformations +
Congenital Cranial Dysinnervation Disorders
Dandy-Walker Syndrome
Hereditary Sensory and Autonomic Neuropathies +
Hereditary Sensory and Motor Neuropathy +
Hydranencephaly
Malformations of Cortical Development +
Neural Tube Defects +
Optic Nerve Hypoplasia +
Respiratory System Abnormalities
Bronchogenic Cyst
Bronchopulmonary Sequestration
Choanal Atresia
Cystic Adenomatoid Malformation of Lung, Congenital
Kartagener Syndrome
Laryngocele
Laryngostenosis
Scimitar Syndrome
Tracheobronchomegaly
Situs Inversus
Dextrocardia +
Levocardia
Skin Abnormalities
Acrodermatitis
Carney Complex
Dyskeratosis Congenita
Ectodermal Dysplasia +
Ehlers-Danlos Syndrome +
Epidermolysis Bullosa +
Ichthyosis +
Incontinentia Pigmenti
Port-Wine Stain
Prolidase Deficiency
Pseudoxanthoma Elasticum
Rothmund-Thomson Syndrome
Sclerema Neonatorum
Trichothiodystrophy Syndromes
Xeroderma Pigmentosum
Stomatognathic System Abnormalities
Maxillofacial Abnormalities +
Mouth Abnormalities +
Tooth Abnormalities +
Thyroid Dysgenesis
Lingual Thyroid +
Urogenital Abnormalities
Bladder Exstrophy
Cryptorchidism
Disorders of Sex Development +
Epispadias
Fraser Syndrome
Fused Kidney
Hypospadias
Multicystic Dysplastic Kidney
Nephritis, Hereditary
Pyelectasis
Retrocaval Ureter
Uterine Duplication Anomalies