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DO Term : isolated microphthalmia 7 [DOID:0060838] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An isolated microphthalmia characterized by unilateral microphthalmia that has_material_basis_in caused by mutation in the GDF3 gene on chromosome 12p13.

synonyms:
OMIM:613704,
ORDO:2542,
MCOP7,
ICD10CM:Q11.0,
613704

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

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