distal trisomy 1p36
Findings
No curated finding names distal trisomy 1p36 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Distal trisomy 1p36 is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the short arm of chromosome 1, characterized by borderline to mild intellectual disability, mild developmental delay, metopic craniosynostosis and mild craniofacial dysmorphism (incl. slopping forehead, bitemporal narrowing, blepharophimosis). Other associated abnormalities may include growth retardation, microcephaly, large hands, syndactyly, supernumerary ribs, rectal stenosis and/or anterior displacement of anus. Congenital heart malformations (e.g. atrial septal defect, patent ductus arteriosus) have also been reported.
Definition from the Mondo Disease Ontology (MONDO:0019870), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
4 names
Resolves to: distal trisomy 1p36
- Also called
- distal duplication 1p36distal trisomy type 1p36telomeric duplication 1p36trisomy 1pter