Hypomagnesemia
Symptom Information:
| Symptom ID: | HPO:0002917 | ||||
| Synonyms: |
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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 magnesium homeostasis(HPO:0004921) Hypomagnesemia(HPO:0002917) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Bone, calcium, magnesium and phosphorus metabolism disorders(MedDRA:10013296) Magnesium metabolism disorders(MedDRA:10025439) Hypomagnesemia(HPO:0002917) |
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| Database Frequency: | 19 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Autosomal dominant primary hypomagnesemia with hypocalcuria | (Orphanet:34528) |
| Autosomal recessive Kenny-Caffey syndrome | (Orphanet:93324) |
| Autosomal recessive primary hypomagnesemia with normocalcuria and hypocalcemia | (Orphanet:30924) |
| BARTTER SYNDROME, ANTENATAL, TYPE 1 | (OMIM:601678) |
| Bartter syndrome | (Orphanet:112) |
| Bartter syndrome with hypocalcemia | (Orphanet:263417) |
| Cronkhite-Canada syndrome | (Orphanet:2930) |
| EAST syndrome | (Orphanet:199343) |
| Familial hypomagnesemia - hypercalciuria - nephrocalcinosis | (Orphanet:31043) |
| Familial hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement | (Orphanet:2196) |
| Familial primary hypomagnesemia with normocalcuria and normocalcemia | (Orphanet:34527) |
| Gaucher disease type 2 | (Orphanet:77260) |
| Gitelman syndrome | (Orphanet:358) |
| HYPOMAGNESEMIA 6, RENAL | (OMIM:613882) |
| Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome | (Orphanet:363694) |
| Kearns-Sayre syndrome | (Orphanet:480) |
| Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
| Renal cysts and diabetes syndrome | (Orphanet:93111) |
| Tubular renal disease-cardiomyopathy syndrome | (Orphanet:73224) |