PomBase home

Disease association ontology term - MONDO:0006573 - lipodystrophy

Term summary

ID
MONDO:0006573
Name
lipodystrophy
Ontology or CV name
Disease association
Definition
A congenital or acquired disorder characterized by abnormal loss or redistribution of the adipose tissue in the body.

Parents

Annotation

Disease association

MONDO:0006573 - lipodystrophy

References:

Genes:

MONDO:0012071 - congenital generalized lipodystrophy type 1

References:

Genes:

MONDO:0010020 - congenital generalized lipodystrophy type 2

References:

Genes:

MONDO:0958023 - lipodystrophy, congenital generalized, type 5

References:

Genes:

MONDO:0012074 - mandibuloacral dysplasia with type B lipodystrophy

References:

Genes:

MONDO:0014402 - severe neurodegenerative syndrome with lipodystrophy

References:

Genes:

MONDO:0009910 - Wiedemann-Rautenstrauch syndrome

References:

Genes: