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DOID:0050819 - Matthew-Wood syndrome
Disease Ontology Definition:An autosomal genetic disease that is characterized by microphthalmia or anophthalmia, pulmonary agenesis, and diaphragmatic defect.
Synonyms: MCOPS9, microphthalmia syndromic type 9 ,
Echinobase Genes :
MIM:601186 - microphthalmia, syndromic 9; mcops9 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal genetic disease (is_a)