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DOID:0060391 - chromosome 13q14 deletion syndrome
Disease Ontology Definition:A chromosomal deletion syndrome that is characterized by low birth weight, dysmorphic facies, limb defects, genital malformations and psychomotor developmental delay, has_material_basis_in deletion of the long arm of chromosome 13.
Synonyms: deletion 13q14,
Xenbase Genes :
MONDO:0013481 - chromosome 13q14 deletion syndrome |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee