Disease #02598

Official abbreviation LCCNS
Name lipodystrophy, partial, congenital cataracts and neurodegeneration (LCCNS)
OMIM ID 606721
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CAV1
Associated tissues -
Disease features -
Remarks -