Hypoparathyroidism

Symptom Information:

Symptom ID: HPO:0000829
Synonyms:
Low parathyroid hormone [HPO:0000829]
Hypoparathyroidism (disorder) [Orphanet:41360]
hypoparathyroidism [HPO:0000829]
Hypoparathyroidism [Orphanet:41360]
Hypoparathyroidism [OMIM:Hypoparathyroidism]
Low parathyroid hormone [OMIM:Low parathyroid hormone]
Hypoparathyroidy [Orphanet:41360]
Hypoparathyroidism [MedDRA:10021041]
Quality:
Cross references:
Orphanet:41360 "Hypoparathyroidy" [Orphanet:41360]
OMIM: "Hypoparathyroidism" [OMIM:Hypoparathyroidism]
OMIM: "Low parathyroid hormone" [OMIM:Low parathyroid hormone]
UMLS:C1384672 "hypoparathyroidism" [HPO:0000829]
UMLS:C0020626 "Hypoparathyroidism" [Orphanet:41360]
Is a (Direct Parents):
MedDRA Endocrine procedural complications
HPO         Abnormality of the parathyroid physiology
Orphanet Abnormality of the parathyroid gland
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)
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)