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Overview
chromosome 15q26-qter deletion syndrome
Ontology Term:
Status:
Live
Synonym:
15q26 deletion syndrome
Drayer syndrome
distal 15q deletion syndrome
distal monosomy 15q
telomeric 15q deletion syndrome
Drayer syndrome
distal 15q deletion syndrome
distal monosomy 15q
telomeric 15q deletion syndrome
Type:
Mapping to OMIM ID:
WormBase ID:
DOID:0060397
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.
Parent:
Child:
Associations based on experimental data:
Disease relevant gene:
Automatic gene association:
1 Inferred automatically: Inferred by orthology to human genes with OMIM annotation