congenital generalized lipodystrophy type 4
congenital generalized lipodystrophy that has material basis in an autosomal recessive mutation of PTRF on chromosome 17q21.2
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congenital generalized lipodystrophy type 4
Summary
congenital generalized lipodystrophy type 4 is a rare disease[1]. It is known by 12 alternative names across languages and contexts.[2]
Key Facts
- congenital generalized lipodystrophy type 4's instance of is recorded as rare disease[3].
- congenital generalized lipodystrophy type 4's instance of is recorded as class of disease[4].
- congenital generalized lipodystrophy type 4 is a type of congenital generalized lipodystrophy[5].
- congenital generalized lipodystrophy type 4 is a type of genetic cardiac rhythm disease[6].
- congenital generalized lipodystrophy type 4 is a type of insulin resistance[7].
- congenital generalized lipodystrophy type 4 is a type of rare genetic diabetes mellitus[8].
- congenital generalized lipodystrophy type 4 is a type of non-dystrophic myopathy[9].
- congenital generalized lipodystrophy type 4 is a type of autosomal recessive disease[10].
- congenital generalized lipodystrophy type 4's genetic association is recorded as CAVIN1[11].
- congenital generalized lipodystrophy type 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111138[12].
- congenital generalized lipodystrophy type 4's exact match is recorded as http://identifiers.org/doid/DOID:0111138[13].
- congenital generalized lipodystrophy type 4's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_228429[14].
- congenital generalized lipodystrophy type 4's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
congenital generalized lipodystrophy type 4 is known by 12 alternative names across languages and contexts.[2]