Pseudohypoparathyroidism type I A
- Synonyms
- Albright hereditary osteodystrophy with multiple hormone resistance; PHP IA; Pseudohypoparathyroidism Ia (PHP-Ia); Pseudohypoparathyroidism Type IA; Pseudohypoparathyroidism type 1A
- Modes of inheritance
- Autosomal dominant inheritance (Orphanet)
Summary
Excerpted from the GeneReview:- Full text of GeneReview (by section):
- Summary
- GeneReview Scope
- Diagnosis
- Clinical Characteristics
- Genetically Related (Allelic) Disorders
- Differential Diagnosis
- Management
- Genetic Counseling
- Resources
- Molecular Genetics
- Chapter Notes
- References
- Authors:
- Chad R Haldeman-Englert
- Anna CE Hurst
- Michael A Levine
- view full author information
Available tests
Check Related conditions for additional relevant tests.
Genes See tests for all associated and related genes
Also known as: AHO, AIMAH1, C20orf45, GNAS1, GPSA, GSA, GSP, NESP, PITA3, POH, SCG6, SgVI, GNAS
Summary: GNAS complex locus
Clinical features
Help- Abnormality of head or neck
- Delayed eruption of teeth
Delayed eruption of teeth
- MedGen UID: 68678
- Concept ID: C0239174
- Finding: Finding
Abnormality of head or neck
- Depressed nasal bridge
Depressed nasal bridge
- MedGen UID: 373112
- Concept ID: C1836542
- Finding: Finding
Abnormality of head or neck
- Enamel hypoplasia
Enamel hypoplasia
- MedGen UID: 3730
- Concept ID: C0011351
- Finding: Disease or Syndrome
Abnormality of head or neck
- Full cheeks
Full cheeks
- MedGen UID: 355661
- Concept ID: C1866231
- Finding: Finding
Abnormality of head or neck
- Round face
Round face
- MedGen UID: 116087
- Concept ID: C0239479
- Finding: Finding
Abnormality of head or neck
- Short neck
Short neck
- MedGen UID: 99267
- Concept ID: C0521525
- Finding: Finding
Abnormality of head or neck
- Delayed eruption of teeth
- Abnormality of limbs
- Brachydactyly
Brachydactyly
- MedGen UID: 67454
- Concept ID: C0221357
- Finding: Congenital Abnormality
Abnormality of limbs
- Short finger
Short finger
- MedGen UID: 334977
- Concept ID: C1844548
- Finding: Anatomical Abnormality
Abnormality of limbs
- Short metacarpal
Short metacarpal
- MedGen UID: 323064
- Concept ID: C1837084
- Finding: Anatomical Abnormality
Abnormality of limbs
- Short metatarsal
Short metatarsal
- MedGen UID: 341358
- Concept ID: C1849020
- Finding: Finding
Abnormality of limbs
- Short toe
Short toe
- MedGen UID: 322858
- Concept ID: C1836195
- Finding: Finding
Abnormality of limbs
- Brachydactyly
- Abnormality of metabolism/homeostasis
- Elevated circulating parathyroid hormone level
Elevated circulating parathyroid hormone level
- MedGen UID: 167805
- Concept ID: C0857973
- Finding: Finding
Abnormality of metabolism/homeostasis
- Hyperphosphatemia
Hyperphosphatemia
- MedGen UID: 39326
- Concept ID: C0085681
- Finding: Disease or Syndrome
Abnormality of metabolism/homeostasis
- Elevated circulating parathyroid hormone level
- Abnormality of the endocrine system
- Hypogonadism
Hypogonadism
- MedGen UID: 5711
- Concept ID: C0020619
- Finding: Disease or Syndrome
Abnormality of the endocrine system
- Hypothyroidism
Hypothyroidism
- MedGen UID: 6991
- Concept ID: C0020676
- Finding: Disease or Syndrome
Abnormality of the endocrine system
- Pseudohypoparathyroidism
Pseudohypoparathyroidism
- MedGen UID: 46178
- Concept ID: C0033806
- Finding: Disease or Syndrome
Abnormality of the endocrine system
- Hypogonadism
- Abnormality of the eye
- Abnormality of the genitourinary system
- Low urinary cyclic AMP response to PTH administration
Low urinary cyclic AMP response to PTH administration
- MedGen UID: 350345
- Concept ID: C1864105
- Finding: Finding
Abnormality of the genitourinary system
- Low urinary cyclic AMP response to PTH administration
- Abnormality of the musculoskeletal system
- Basal ganglia calcification
Basal ganglia calcification
- MedGen UID: 234651
- Concept ID: C1389280
- Finding: Pathologic Function
Abnormality of the musculoskeletal system
- Choroid plexus calcification
Choroid plexus calcification
- MedGen UID: 354924
- Concept ID: C1863184
- Finding: Pathologic Function
Abnormality of the musculoskeletal system
- Osteoporosis
Osteoporosis
- MedGen UID: 14535
- Concept ID: C0029456
- Finding: Disease or Syndrome
Abnormality of the musculoskeletal system
- Subcutaneous ossification
Subcutaneous ossification
- MedGen UID: 811667
- Concept ID: C3805337
- Finding: Finding
Abnormality of the musculoskeletal system
- Thickened calvaria
Thickened calvaria
- MedGen UID: 346823
- Concept ID: C1858452
- Finding: Finding
Abnormality of the musculoskeletal system
- Basal ganglia calcification
- Abnormality of the nervous system
- Cognitive impairment
Cognitive impairment
- MedGen UID: 90932
- Concept ID: C0338656
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Hypocalcemic tetany
Hypocalcemic tetany
- MedGen UID: 57499
- Concept ID: C0151940
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Intellectual disability
Intellectual disability
- MedGen UID: 811461
- Concept ID: C3714756
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Seizure
Seizure
- MedGen UID: 20693
- Concept ID: C0036572
- Finding: Sign or Symptom
Abnormality of the nervous system
- Cognitive impairment
- Growth abnormality
- Obesity
Obesity
- MedGen UID: 18127
- Concept ID: C0028754
- Finding: Disease or Syndrome
Growth abnormality
- Short stature
Short stature
- MedGen UID: 87607
- Concept ID: C0349588
- Finding: Finding
Growth abnormality
- Obesity
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