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Summary Literature (0)
MIM:609508 - STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR

Xenbase Genes: col2a1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007160 - Stickler syndrome type 1
MONDO:0012287 - Stickler syndrome, type I, nonsyndromic ocular
MONDO:0016202 - autosomal dominant rhegmatogenous retinal detachment
MONDO:0019354 - Stickler syndrome