Term Name: syndromic microphthalmia 12
Synonyms: MCOPS12, microphthalmia with or without pulmonary hypoplasia, diaphragmatic hernia, and/or cardiac defects
Definition: A syndromic microphthalmia characterized by bilateral microphthalmia, pulmonary hypoplasia, and diaphragmatic hernia that has_material_basis_in compound heterozygous or heterozygous mutation in the RARB gene on chromosome 3p24.2.
Ontology: Human Disease [DOID:0111800]   ( DOID:0111800 )

Relationships
is a type of: autosomal genetic disease syndromic microphthalmia