chromosome 1p35 deletion syndrome
MONDO:0060677Mondo
Findings
No curated finding names chromosome 1p35 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 · Third trimester onset
HPO, annotations 2026-09-02
Features
30 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.
- Almond-shaped palpebral fissureHPOHP:0007874
- 2 of 2 reported patients
- Feeding difficultiesHPOHP:0011968
- 2 of 2 reported patients
- Global developmental delayHPOHP:0001263
- 2 of 2 reported patients
- Hearing impairmentHPOHP:0000365
- 2 of 2 reported patients
- HypermetropiaHPOHP:0000540
- 2 of 2 reported patients
- Myopathic faciesHPOHP:0002058
- 2 of 2 reported patients
- Narrow mouthHPOHP:0000160
- 2 of 2 reported patients
- Prominent foreheadHPOHP:0011220
- 2 of 2 reported patients
- Thin upper lip vermilionHPOHP:0000219
- 2 of 2 reported patients
- Absent speechHPOHP:0001344
- 1 of 2 reported patients
- Anterior creases of earlobeHPOHP:0009908
- 1 of 2 reported patients
- Breech presentationHPOHP:0001623
- 1 of 2 reported patients
Show the remaining 18
- Clinodactyly of the 5th fingerHPOHP:0004209
- 1 of 2 reported patients
- Congenital hypothyroidismHPOHP:0000851
- 1 of 2 reported patients
- CoughHPOHP:0012735
- 1 of 2 reported patients
- Delayed gross motor developmentHPOHP:0002194
- 1 of 2 reported patients
- DysarthriaHPOHP:0001260
- 1 of 2 reported patients
- EsophoriaHPOHP:0025312
- 1 of 2 reported patients