Disease #03646 (ADCL2 (cutis laxa, autosomal dominant, type 2 (ADCL-2)), OMIM:614434)

Official abbreviation ADCL2
Name cutis laxa, autosomal dominant, type 2 (ADCL-2)
OMIM ID 614434
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FBLN5
Associated tissues -
Disease features -
Remarks -