About   Help   FAQ
Disease Ontology Browser
chromosome 15q26-qter deletion syndrome (DOID:0060397)
Alliance: disease page
Synonyms: 15q26 deletion syndrome; distal 15q deletion syndrome; distal monosomy 15q; Drayer syndrome; telomeric 15q deletion syndrome
Alt IDs: OMIM:612626, ICD10CM:Q93.5, MESH:C567232, ORDO:1596
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory