Abnormality of calcium homeostasis
Symptom Information:
Symptom ID: | HPO:0004363 | ||||
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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) MedDRA: |
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Database Frequency: | 4 / 7739 | ||||
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All diseases associated with this symptom:
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |
[DEL] NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4 | (OMIM:612541) |