WormBase Tree Display for DO_term: DOID:0111811
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DOID:0111811 | Name | syndromic microphthalmia 13 | |||
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Status | Valid | ||||
Definition | A syndromic microphthalmia characterized by colobomatous microphthalmia, microcephaly, short stature, and psychomotor retardation that has_material_basis_in mutation in the HMGB3 gene on chromosome Xq28. | ||||
Synonym | Exact | MCOPS13 | |||
Maine microphthalmos | |||||
X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome | |||||
colobomatous microphthalmia with microcephaly, short stature, and psychomotor retardation | |||||
Parent | Is_a (2) | ||||
DB_info | Database | OMIM | disease | 300915 | |
Attribute_of | Gene_by_orthology | WBGene00001972 |