You are using an outdated browser. Please upgrade your browser to improve your experience.

autosomal recessive cutis laxa type 1

Disease Summary
Associated Targets (3)
Tbio

2

Tchem

1


GARD Rare
Mondo Description Autosomal recessive cutis laxa, type 1 (ARCL1) is a generalized connective tissue disorder characterized by the association of wrinkled, redundant and sagging inelastic skin with severe systemic manifestations (lung atelectesias and emphysema, vascular anomalies, and gastrointestinal and genitourinary tract diverticuli).
Mondo Term and Equivalent IDs
MONDO:0019572:  autosomal recessive cutis laxa type 1
GARD:0008480: 
MESH:C536225: 
Orphanet:90349: 
SCTID:254222002: 
UMLS:CN206407: