congenital generalized lipodystrophy type 3
congenital generalized lipodystrophy that has material basis in an autosomal recessive mutation of CAV1 on chromosome 7q31.2
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congenital generalized lipodystrophy type 3
Summary
congenital generalized lipodystrophy type 3 is a rare disease[1].
Key Facts
- congenital generalized lipodystrophy type 3's instance of is recorded as rare disease[2].
- congenital generalized lipodystrophy type 3's instance of is recorded as class of disease[3].
- congenital generalized lipodystrophy type 3's subclass of is recorded as congenital generalized lipodystrophy[4].
- congenital generalized lipodystrophy type 3's MeSH descriptor ID is recorded as C567282[5].
- congenital generalized lipodystrophy type 3's OMIM ID is recorded as 612526[6].
- congenital generalized lipodystrophy type 3's OMIM ID is recorded as 612526[7].
- congenital generalized lipodystrophy type 3's Disease Ontology ID is recorded as DOID:0111137[8].
- congenital generalized lipodystrophy type 3's genetic association is recorded as CAV1[9].
- congenital generalized lipodystrophy type 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111137[10].
- congenital generalized lipodystrophy type 3's exact match is recorded as http://identifiers.org/doid/DOID:0111137[11].
- congenital generalized lipodystrophy type 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_528[12].
- congenital generalized lipodystrophy type 3's UMLS CUI is recorded as C2675861[13].
- congenital generalized lipodystrophy type 3's ICD-10-CM is recorded as E88.1[14].
- congenital generalized lipodystrophy type 3's GARD rare disease ID is recorded as 13389[15].
- congenital generalized lipodystrophy type 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- congenital generalized lipodystrophy type 3's Mondo ID is recorded as MONDO_0012923[17].
- congenital generalized lipodystrophy type 3's UniProt disease ID is recorded as DI-00356[18].