OBO ID: DOID:0060839
Term Name: isolated microphthalmia 2 Search Ontology:
Synonyms:
  • MCOP2
Definition: A 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. (2)
References:
Ontology: Human Disease   (DOID:0060839)
Relationships
is a type of:
OTHER isolated microphthalmia 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
VSX2 Microphthalmia, isolated 2 610093
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None