autosomal dominant hypocalcemia 2
autosomal dominant hypocalcemia disease that has material basis in heterozygous mutation in the GNA11 gene on chromosome 19p13
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autosomal dominant hypocalcemia 2
Summary
autosomal dominant hypocalcemia 2 is a rare disease[1].
Key Facts
- autosomal dominant hypocalcemia 2's instance of is recorded as rare disease[2].
- autosomal dominant hypocalcemia 2's instance of is recorded as class of disease[3].
- autosomal dominant hypocalcemia 2's subclass of is recorded as autosomal dominant hypocalcemia[4].
- autosomal dominant hypocalcemia 2's OMIM ID is recorded as 615361[5].
- autosomal dominant hypocalcemia 2's Disease Ontology ID is recorded as DOID:0090108[6].
- autosomal dominant hypocalcemia 2's genetic association is recorded as GNA11[7].
- autosomal dominant hypocalcemia 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090108[8].
- autosomal dominant hypocalcemia 2's exact match is recorded as http://identifiers.org/doid/DOID:0090108[9].
- autosomal dominant hypocalcemia 2's UMLS CUI is recorded as C3809243[10].
- autosomal dominant hypocalcemia 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
- autosomal dominant hypocalcemia 2's Mondo ID is recorded as MONDO_0014146[12].
- autosomal dominant hypocalcemia 2's UniProt disease ID is recorded as DI-03851[13].