trisomy 10p
MONDO:0015761Mondo
Findings
No curated finding names trisomy 10p yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Trisomy 10p is a syndrome of mental retardation/multiple congenital malformations (MR-MCA) that is caused by the total or partial duplication of the short arm of chromosome 10.
Definition from the Mondo Disease Ontology (MONDO:0015761), read 2026-09-29. CC BY 4.0.
Features
63 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Growth delayHPOHP:0001510
- Very frequent (80% to 99% of cases)
- Intellectual disabilityHPOHP:0001249
- Very frequent (80% to 99% of cases)
- Intrauterine growth retardationHPOHP:0001511
- Very frequent (80% to 99% of cases)
- Small for gestational ageHPOHP:0001518
- Very frequent (80% to 99% of cases)
- Abnormal facial shapeHPOHP:0001999
- Frequent (30% to 79% of cases)
- Abnormal foot morphologyHPOHP:0001760
- Frequent (30% to 79% of cases)
- Abnormal lip morphologyHPOHP:0000159
- Frequent (30% to 79% of cases)
- Abnormality of the earHPOHP:0000598
- Frequent (30% to 79% of cases)
- Abnormality of the eyeHPOHP:0000478
- Frequent (30% to 79% of cases)
- Abnormality of the genitourinary systemHPOHP:0000119
- Frequent (30% to 79% of cases)
- Abnormality of the handHPOHP:0001155
- Frequent (30% to 79% of cases)
- Abnormality of the noseHPOHP:0000366
- Frequent (30% to 79% of cases)
Show the remaining 51
- Abnormality of the skeletal systemHPOHP:0000924
- Frequent (30% to 79% of cases)
- DolichocephalyHPOHP:0000268
- Frequent (30% to 79% of cases)
- High foreheadHPOHP:0000348
- Frequent (30% to 79% of cases)
- HypertelorismHPOHP:0000316
- Frequent (30% to 79% of cases)
- Prominent foreheadHPOHP:0011220
- Frequent (30% to 79% of cases)
- SeizureHPOHP:0001250
- Frequent (30% to 79% of cases)
Where it sits
Other names
1 name
Resolves to: trisomy 10p
- Also called
- trisomy type 10p