Disease #00059 (EDSCL2 (EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2), OMIM:130010)

Official abbreviation EDSCL2
Name EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2
OMIM ID 130010
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 2 genes AEBP1, COL5A2
Associated tissues -
Disease features -
Remarks -

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