Hypocalcemia

Symptom Information:

Symptom ID: HPO:0002901
Synonyms:
Hypocalcaemia [HPO:0002901]
Hypocalcemia (disorder) [Orphanet:49240]
HYPOCALCAEMIA [HPO:0002901]
Hypocalcemia [Orphanet:49240]
Hypocalcemia [OMIM:Hypocalcemia]
Blood calcium decreased [Orphanet:49240]
Hypocalcaemia [Orphanet:49240]
Blood calcium decreased [MedDRA:10005395]
Ca level lowered [MedDRA:10005395]
Ca++ decreased [MedDRA:10005395]
Calcium blood decreased [MedDRA:10005395]
Calcium decreased [MedDRA:10005395]
Calcium low [MedDRA:10005395]
Calcium serum decreased [MedDRA:10005395]
Calcium total decreased [MedDRA:10005395]
Plasma calcium decreased [MedDRA:10005395]
Serum calcium decreased [MedDRA:10005395]
Hypocalcaemia [MedDRA:10020947]
Hypocalcemia [MedDRA:10020947]
Hypocalcemia (64% of adults) [OMIM:Hypocalcemia (64% of adults)]
Hypocalcemia (male) [OMIM:Hypocalcemia (male)]
Quality:
Cross references:
Orphanet:49240 "Hypocalcemia" [Orphanet:49240]
OMIM: "Hypocalcemia" [OMIM:Hypocalcemia]
OMIM: "Hypocalcemia (64% of adults)" [OMIM:Hypocalcemia (64% of adults)]
OMIM: "Hypocalcemia (male)" [OMIM:Hypocalcemia (male)]
UMLS:C0020598 "HYPOCALCAEMIA" [HPO:0002901]
UMLS:C0020598 "Hypocalcemia" [Orphanet:49240]
Is a (Direct Parents):
MedDRA Calcium metabolism disorders
HPO         Abnormality of calcium homeostasis
Orphanet Abnormality of calcium-phosphate metabolism
MedDRA Mineral and electrolyte analyses
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)
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)