Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
OMIM:606721 - LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 7; FPLD7


Xenbase Genes: cav1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011714 - partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome