cortisone reductase deficiency 2
cortisone reductase deficiency that has material basis in heterozygous mutation in the HSD11B1 gene on chromosome 1q32
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cortisone reductase deficiency 2
Summary
cortisone reductase deficiency 2 is a rare disease[1].
Key Facts
- cortisone reductase deficiency 2's instance of is recorded as rare disease[2].
- cortisone reductase deficiency 2's instance of is recorded as class of disease[3].
- cortisone reductase deficiency 2 is a type of cortisone reductase deficiency[4].
- cortisone reductase deficiency 2 is a type of genetic disease[5].
- cortisone reductase deficiency 2 is a type of autosomal dominant disease[6].
- cortisone reductase deficiency 2's NCI Thesaurus ID is recorded as C131084[7].
- cortisone reductase deficiency 2's genetic association is recorded as HSD11B1[8].
- cortisone reductase deficiency 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090140[9].
- cortisone reductase deficiency 2's exact match is recorded as http://identifiers.org/doid/DOID:0090140[10].
- cortisone reductase deficiency 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].