Hypoparathyroidism
Symptom Information:
Symptom ID: | HPO:0000829 | ||||||||
Synonyms: |
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Quality: | |||||||||
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) Hypoparathyroidism(HPO:0000829) MedDRA: Injury, poisoning and procedural complications(MedDRA:10022117) Procedural related injuries and complications NEC(MedDRA:10069888) Endocrine procedural complications(MedDRA:10014716) Hypoparathyroidism(HPO:0000829) |
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Database Frequency: | 22 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
22q11.2 deletion syndrome | (Orphanet:567) |
Autoimmune polyendocrinopathy type 1 | (Orphanet:3453) |
Autoimmune polyendocrinopathy type 2 | (Orphanet:3143) |
Autosomal dominant Kenny-Caffey syndrome | (Orphanet:93325) |
Autosomal recessive Kenny-Caffey syndrome | (Orphanet:93324) |
Beta-thalassemia major | (Orphanet:231214) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Dahlberg-Borer-Newcomer syndrome | (Orphanet:1563) |
Dubowitz syndrome | (Orphanet:235) |
Familial isolated hypoparathyroidism | (Orphanet:2238) |
Familial isolated hypoparathyroidism due to agenesis of parathyroid gland | (Orphanet:2239) |
Familial isolated hypoparathyroidism due to impaired PTH secretion | (Orphanet:189466) |
Hypoparathyroidism - deafness - renal disease | (Orphanet:2237) |
Kearns-Sayre syndrome | (Orphanet:480) |
Kenny-Caffey syndrome | (Orphanet:2333) |
MELAS | (Orphanet:550) |
Metaphyseal chondrodysplasia, Jansen type | (Orphanet:33067) |
Microlissencephaly - micromelia | (Orphanet:50810) |
Navajo neurohepatopathy | (Orphanet:255229) |
Sanjad-Sakati syndrome | (Orphanet:2323) |
Wilson disease | (Orphanet:905) |
X-linked Alport syndrome | (Orphanet:88917) |