Visualize Submit Comment
Metadata
ID DOID:0060255
Name rippling muscle disease 2
Definition A muscle tissue disease characterized by mechanically triggered contractions of skeletal muscle and that has_material_basis_in mutation in the caveolin-3 gene (CAV3) on chromosome 3p25.
https://www.ncbi.nlm.nih.gov/pubmed/9537420, http://ghr.nlm.nih.gov/condition/rippling-muscle-disease
Xrefs

GARD:9164

MIM:606072

ORDO:265

ORDO:97238

SNOMEDCT_US_2023_03_01:709281006

UMLS_CUI:C1853698

Alternateids

DOID:0110302

Subsets

DO_rare_slim

Synonyms

autosomal dominant limb-girdle muscular dystrophy type 1C [EXACT]

Parent Relationships

is_a autosomal dominant disease

is_a muscle tissue disease

Subclass Logical Relationships

has material basis in some autosomal dominant inheritance

Add an item to the term tracker