chromosome 1p36 deletion syndrome, proximal
MONDO:0859155Mondo
Findings
No curated finding names chromosome 1p36 deletion syndrome, proximal yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance · Contiguous gene syndrome
- Onset and course
- Infantile onset · Neonatal onset · Fetal onset
HPO, annotations 2026-09-02
Features
35 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.
- Anteverted naresHPOHP:0000463
- 5 of 5 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 3 of 3 reported patients
- Failure to thriveHPOHP:0001508
- 5 of 5 reported patients
- Global developmental delayHPOHP:0001263
- 5 of 5 reported patients
- HypotoniaHPOHP:0001252
- 5 of 5 reported patients
- Low-set earsHPOHP:0000369
- 5 of 5 reported patients
- Posteriorly rotated earsHPOHP:0000358
- 5 of 5 reported patients
- Broad eyebrowHPOHP:0011229
- 4 of 5 reported patients
- EpicanthusHPOHP:0000286
- 4 of 5 reported patients
- HirsutismHPOHP:0001007
- 4 of 5 reported patients
- MicrocephalyHPOHP:0000252
- 4 of 5 reported patients
- ClinodactylyHPOHP:0030084
- 3 of 5 reported patients
Show the remaining 23
- Frontal bossingHPOHP:0002007
- 3 of 5 reported patients
- MicrognathiaHPOHP:0000347
- 3 of 5 reported patients
- Midface retrusionHPOHP:0011800
- 3 of 5 reported patients
- Parietal bossingHPOHP:0000242
- 3 of 5 reported patients
- Pointed chinHPOHP:0000307
- 3 of 5 reported patients
- SeizureHPOHP:0001250
- 3 of 5 reported patients
Where it sits
- A kind of