glucocorticoid deficiency 2
human disease
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glucocorticoid deficiency 2
Summary
glucocorticoid deficiency 2 is a rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- glucocorticoid deficiency 2's instance of is recorded as rare disease[3].
- glucocorticoid deficiency 2's instance of is recorded as disease[4].
- glucocorticoid deficiency 2 is a type of familial glucocorticoid deficiency[5].
- glucocorticoid deficiency 2's symptoms and signs is recorded as failure to thrive[6].
- glucocorticoid deficiency 2's symptoms and signs is recorded as hypotension[7].
- glucocorticoid deficiency 2's symptoms and signs is recorded as hyperpigmentation[8].
- glucocorticoid deficiency 2's NCI Thesaurus ID is recorded as C123728[9].
- glucocorticoid deficiency 2's genetic association is recorded as MRAP[10].
- glucocorticoid deficiency 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_361[11].
- glucocorticoid deficiency 2's has phenotype is recorded as Decreased circulating cortisol level[12].
- glucocorticoid deficiency 2's has phenotype is recorded as Abnormality of circulating adrenocorticotropin level[13].
Why It Matters
glucocorticoid deficiency 2 is known by 5 alternative names across languages and contexts.[2]