chromosome 2p12-p11.2 deletion syndrome
MONDO:0013309Mondo
Findings
No curated finding names chromosome 2p12-p11.2 deletion syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Contiguous gene syndrome
- Onset and course
- Congenital onset · Infantile onset
HPO, annotations 2026-09-02
Features
33 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.
- Aggressive behaviorHPOHP:0000718
- 1 of 1 reported patient
- Anteverted naresHPOHP:0000463
- 1 of 1 reported patient
- BlepharophimosisHPOHP:0000581
- 1 of 1 reported patient
- Clinodactyly of the 4th fingerHPOHP:0040025
- 1 of 1 reported patient
- Conductive hearing impairmentHPOHP:0000405
- 1 of 1 reported patient
- Coronal hypospadiasHPOHP:0008743
- 1 of 1 reported patient
- CryptorchidismHPOHP:0000028
- 1 of 1 reported patient
- Downslanted palpebral fissuresHPOHP:0000494
- 1 of 1 reported patient
- Feeding difficultiesHPOHP:0011968
- 2 of 2 reported patients
- Gait ataxiaHPOHP:0002066
- 1 of 1 reported patient
- Global developmental delayHPOHP:0001263
- 1 of 1 reported patient
- High palateHPOHP:0000218
- 1 of 1 reported patient
Show the remaining 21
- Highly arched eyebrowHPOHP:0002553
- 1 of 1 reported patient
- Intrauterine growth retardationHPOHP:0001511
- 1 of 1 reported patient
- Large fontanellesHPOHP:0000239
- 1 of 1 reported patient
- Low-set earsHPOHP:0000369
- 2 of 2 reported patients
- Lower limb hypertoniaHPOHP:0006895
- 1 of 1 reported patient
- MicrognathiaHPOHP:0000347
- 1 of 1 reported patient