acid-labile subunit deficiency
hereditary disease of the endocrine system
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acid-labile subunit deficiency
Summary
acid-labile subunit deficiency is a rare disease[1].
Key Facts
- acid-labile subunit deficiency's instance of is recorded as rare disease[2].
- acid-labile subunit deficiency's instance of is recorded as class of disease[3].
- acid-labile subunit deficiency's subclass of is recorded as growth hormone insensitivity syndrome[4].
- acid-labile subunit deficiency's OMIM ID is recorded as 615961[5].
- acid-labile subunit deficiency's KEGG ID is recorded as H01907[6].
- acid-labile subunit deficiency's Orphanet ID is recorded as 140941[7].
- acid-labile subunit deficiency's genetic association is recorded as IGFALS[8].
- acid-labile subunit deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_140941[9].
- acid-labile subunit deficiency's UMLS CUI is recorded as C3900122[10].
- acid-labile subunit deficiency's UMLS CUI is recorded as C4303612[11].
- acid-labile subunit deficiency's ICD-10-CM is recorded as E34.3[12].
- acid-labile subunit deficiency's Mondo ID is recorded as MONDO_0014420[13].
- acid-labile subunit deficiency's UniProt disease ID is recorded as DI-04198[14].