Warburg micro syndrome Warburg micro syndrome 1 DOID:0110716 A Warburg micro syndrome characterized by microcephaly, microphthalmia, microcornea, congenital cataracts, optic atrophy, cortical dysplasia, in particular corpus callosum hypoplasia, severely impaired intellectual development, spastic diplegia, and hypogonadism that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP1 gene on chromosome 2q21. MIM:600118 disease_ontology ICD10CM:Q87.0 Micro Syndrome 1 WARBM1