Pseudohypoparathyroidism

Symptom Information:

Symptom ID: HPO:0000852
Synonyms:
Pseudohypoparathyroidism [OMIM:Pseudohypoparathyroidism]
Pseudohypoparathyroidism [MedDRA:10037126]
Quality:
Cross references:
OMIM: "Pseudohypoparathyroidism" [OMIM:Pseudohypoparathyroidism]
UMLS:C0033806 "Pseudohypoparathyroidism" [HPO:0000852]
Is a (Direct Parents):
HPO         Abnormality of the parathyroid physiology
MedDRA Endocrine disorders congenital NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          Abnormality of the parathyroid gland(HPO:0000828)
             Abnormality of the parathyroid physiology(HPO:0011767)
                Pseudohypoparathyroidism(HPO:0000852)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Endocrine disorders congenital(MedDRA:10014699)
       Endocrine disorders congenital NEC(MedDRA:10027671)
          Pseudohypoparathyroidism(HPO:0000852)
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Albright hereditary osteodystrophy (Orphanet:665)
Pseudohypoparathyroidism type 1A (Orphanet:79443)
Pseudohypoparathyroidism type 1B (Orphanet:94089)
Pseudohypoparathyroidism type 1C (Orphanet:79444)
Pseudohypoparathyroidism type 2 (Orphanet:94090)
Pseudopseudohypoparathyroidism (Orphanet:79445)