Pseudohypoparathyroidism
Symptom Information:
Symptom ID: | HPO:0000852 | ||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |