autosomal dominant hypocalcemia
calcium metabolism disease characterized by autosomal dominant inheritance of variable degrees of hypocalcemia with normal to low levels of parathyroid hormone
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autosomal dominant hypocalcemia
Summary
autosomal dominant hypocalcemia is a class of disease[1].
Key Facts
- autosomal dominant hypocalcemia's instance of is recorded as class of disease[2].
- autosomal dominant hypocalcemia's subclass of is recorded as hypocalcaemia[3].
- autosomal dominant hypocalcemia's subclass of is recorded as autosomal dominant disease[4].
- autosomal dominant hypocalcemia's subclass of is recorded as metal metabolism disorder[5].
- autosomal dominant hypocalcemia's MeSH descriptor ID is recorded as C562783[6].
- autosomal dominant hypocalcemia's Disease Ontology ID is recorded as DOID:0090109[7].
- autosomal dominant hypocalcemia's Orphanet ID is recorded as 428[8].
- autosomal dominant hypocalcemia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090109[9].
- autosomal dominant hypocalcemia's exact match is recorded as http://identifiers.org/doid/DOID:0090109[10].
- autosomal dominant hypocalcemia's UMLS CUI is recorded as C0342345[11].
- autosomal dominant hypocalcemia's UMLS CUI is recorded as C4048195[12].
- autosomal dominant hypocalcemia's ICD-10-CM is recorded as E20.8[13].
- autosomal dominant hypocalcemia's GARD rare disease ID is recorded as 2877[14].
- autosomal dominant hypocalcemia's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- autosomal dominant hypocalcemia's Genetics Home Reference Conditions ID is recorded as autosomal-dominant-hypocalcemia[16].