Search Ontology:
Human Disease
syndromic microphthalmia 9
- Term ID
- DOID:0111807
- Synonyms
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- anophthalmia-pulmonary hypoplasia syndrome
- anophthalmia/microphthalmia and pulmonary hypoplasia
- clinical anophthalmia mild facial dysmorphism lung heart and diaphragm malformations
- Matthew-Wood syndrome
- pulmonary agenesis microphthalmi and diaphragmatic defect
- spear syndrome
- Definition
- A syndromic microphthalmia characterized by bilateral clinical anophthalmia, pulmonary hypoplasia or aplasia, cardiac malformations, and diaphragmatic defects that has_material_basis_in homozygous or compound heterozygous mutation in the STRA6 gene on chromosome 15q24.1. (3)
- References
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- MESH:C537768
- MIM:601186
- ORDO:2470
- SNOMEDCT_US_2023_03_01:722458000
- UMLS_CUI:C1832661
- Ontology
- Human Disease ( DOID:0111807 )
- is a type of
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Genes Involved
Zebrafish Models