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DO Term : syndromic microphthalmia 10 [DOID:0111812] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A syndromic microphthalmia characterized by congenital microphthalmia and blindness, microcephaly, progressive spasticity, seizures, progressive atrophy of the brain and profound intellectual disability.
  • synonyms:
  • ORDO:77299,
  • GARD:9292,
  • MCOPS10,
  • MOBA,
  • OMIM:611222,
  • microphthalmia-brain atrophy syndrome,
  • 611222
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents