chromosome 15q25 deletion syndrome
MONDO:0013672Mondo
Findings
No curated finding names chromosome 15q25 deletion syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Congenital onset
HPO, annotations 2026-09-02
Features
19 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.
- CryptorchidismHPOHP:0000028
- 2 of 3 reported patients
- Global developmental delayHPOHP:0001263
- 2 of 3 reported patients
- Congenital diaphragmatic herniaHPOHP:0000776
- 3 of 5 reported patients
- Short neckHPOHP:0000470
- 2 of 5 reported patients
- Webbed neckHPOHP:0000465
- 2 of 5 reported patients
- Hypoplasia of the corpus callosumHPOHP:0002079
- 1 of 3 reported patients
- Cleft palateHPOHP:0000175
- 1 of 5 reported patients
- Coronary artery fistulaHPOHP:0011641
- 1 of 5 reported patients
- Dilatation of renal calicesHPOHP:0100581
- 1 of 5 reported patients
- Flat occiputHPOHP:0005469
- 1 of 5 reported patients
- Inguinal herniaHPOHP:0000023
- 1 of 5 reported patients
- Intrauterine growth retardationHPOHP:0001511
- 1 of 5 reported patients
Show the remaining 7
- Low-set earsHPOHP:0000369
- 1 of 5 reported patients
- Pectus excavatumHPOHP:0000767
- 1 of 5 reported patients
- PolyspleniaHPOHP:0001748
- 1 of 5 reported patients
- Posteriorly rotated earsHPOHP:0000358
- 1 of 5 reported patients
- SynophrysHPOHP:0000664
- 1 of 5 reported patients
- Thin vermilion borderHPOHP:0000233
- 1 of 5 reported patients