Disease #03902 (Ehlers-Danlos syndrome, progeroid type, 2, OMIM:615349)

Official abbreviation -
Name Ehlers-Danlos syndrome, progeroid type, 2
OMIM ID 615349
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene B3GALT6
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A