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Summary Literature (0)
MIM:212720 - MARTSOLF SYNDROME 1; MARTS1

Xenbase Genes: rab3gap2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008929 - obsolete cataract-intellectual disability-hypogonadism syndrome
MONDO:8000008 - Martsolf syndrome 1

Disease Ontology (DO):
DOID:0111586 - Martsolf syndrome