Summary Literature (0)

DOID:0060397 - chromosome 15q26-qter deletion syndrome

Disease Ontology Definition:A chromosomal deletion syndrome that is characterized by pre- and postnatal growth restriction, developmental delay, variable degrees of intellectual disability, brachy-clinodactyly, talipes equinovarus, nail hypoplasia, proximally placed digits and mild craniofacial dysmorphism including microcephaly, triangular face, broad nasal bridge and micrognathia.

Synonyms: 15q26 deletion syndrome, distal 15q deletion syndrome, distal monosomy 15q, Drayer syndrome, telomeric 15q deletion syndrome

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012964 - chromosome 15q26-qter deletion syndrome

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee