isolated microphthalmia 2 (DOID:0060839)
Alliance: disease page
Synonyms: MCOP2
Alt IDs: OMIM:610093, ICD10CM:Q11.0, ORDO:2542
Definition: An isolated microphthalmia characterized by autosomal recessive inheritance of bilateral profound microphthalmia without associated anomalies and with normal intelligence that has_material_basis_in homozygous mutation in the CHX10 gene on chromosome 14q24.