Hypocalcemia
Symptom Information:
Symptom ID: | HPO:0002901 | |||||||||||||||||||||
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 metabolism/homeostasis(HPO:0001939) Abnormality of ion homeostasis(HPO:0003111) Abnormality of cation homeostasis(HPO:0010929) Abnormality of divalent inorganic cation homeostasis(HPO:0010927) Abnormality of calcium homeostasis(HPO:0004363) Hypocalcemia(HPO:0002901) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Bone, calcium, magnesium and phosphorus metabolism disorders(MedDRA:10013296) Calcium metabolism disorders(MedDRA:10006975) Hypocalcemia(HPO:0002901) Investigations(MedDRA:10022891) Water, electrolyte and mineral investigations(MedDRA:10047843) Mineral and electrolyte analyses(MedDRA:10027637) Hypocalcemia(HPO:0002901) |
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Database Frequency: | 56 / 7739 | |||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
22q11.2 deletion syndrome | (Orphanet:567) |
2p21 microdeletion syndrome | (Orphanet:163693) |
Albers-Schönberg osteopetrosis | (Orphanet:53) |
Alpha heavy-chain disease | (Orphanet:100025) |
Autosomal dominant distal renal tubular acidosis | (Orphanet:93608) |
Autosomal dominant hypocalcemia | (Orphanet:428) |
Autosomal recessive Kenny-Caffey syndrome | (Orphanet:93324) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
Autosomal recessive primary hypomagnesemia with normocalcuria and hypocalcemia | (Orphanet:30924) |
Bartter syndrome with hypocalcemia | (Orphanet:263417) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
CHARGE syndrome | (Orphanet:138) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
DIGEORGE SYNDROME | (OMIM:188400) |
Dahlberg-Borer-Newcomer syndrome | (Orphanet:1563) |
Diabetic embryopathy | (Orphanet:1926) |
Distal renal tubular acidosis | (Orphanet:18) |
Familial cutaneous collagenoma | (Orphanet:53296) |
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) |
Gaucher disease type 2 | (Orphanet:77260) |
HYPOCALCEMIA, AUTOSOMAL DOMINANT 2 | (OMIM:615361) |
Hennekam syndrome | (Orphanet:2136) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Hypoparathyroidism - deafness - renal disease | (Orphanet:2237) |
Intellectual deficit, X-linked - craniofacioskeletal syndrome | (Orphanet:163979) |
Intestinal lymphangiectasia | (Orphanet:36204) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
Kenny-Caffey syndrome | (Orphanet:2333) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3 | (OMIM:612526) |
MYOPATHY, TUBULAR AGGREGATE, 2 | (OMIM:615883) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Osteocraniostenosis | (Orphanet:2763) |
Osteopetrosis | (Orphanet:2781) |
Pearson syndrome | (Orphanet:699) |
Primary Fanconi syndrome | (Orphanet:3337) |
Primary intestinal lymphangiectasia | (Orphanet:90362) |
Progressive familial intrahepatic cholestasis | (Orphanet:172) |
Pseudohypoparathyroidism type 1A | (Orphanet:79443) |
Pseudohypoparathyroidism type 1B | (Orphanet:94089) |
Pseudohypoparathyroidism type 1C | (Orphanet:79444) |
Pseudohypoparathyroidism type 2 | (Orphanet:94090) |
Ring chromosome 10 | (Orphanet:1438) |
Sanjad-Sakati syndrome | (Orphanet:2323) |
Secondary intestinal lymphangiectasia | (Orphanet:90363) |
Timothy syndrome | (Orphanet:65283) |
VELOCARDIOFACIAL SYNDROME | (OMIM:192430) |
VISCERAL STEATOSIS, CONGENITAL | (OMIM:228100) |
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A | (OMIM:264700) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2A | (OMIM:277440) |