Ververi-Brady syndrome 2
MONDO:0980726Mondo
Findings
No curated finding names Ververi-Brady syndrome 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
28 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.
- Global developmental delayHPOHP:0001263
- 8 of 8 reported patients
- HypotoniaHPOHP:0001252
- 7 of 8 reported patients
- Muscle weaknessHPOHP:0001324
- 7 of 8 reported patients
- Feeding difficultiesHPOHP:0011968
- 6 of 7 reported patients
- Intellectual disabilityHPOHP:0001249
- 3 of 4 reported patients
- Cupped earHPOHP:0000378
- 3 of 5 reported patients
- AnkyloglossiaHPOHP:0010296
- 4 of 7 reported patients
- Postnatal growth retardationHPOHP:0008897
- 5 of 9 reported patients
- Deeply set eyeHPOHP:0000490
- 2 of 5 reported patients
- Low-set earsHPOHP:0000369
- 2 of 5 reported patients
- PtosisHPOHP:0000508
- 2 of 5 reported patients
- Thickened helicesHPOHP:0000391
- 2 of 5 reported patients
Show the remaining 16
- Thin vermilion borderHPOHP:0000233
- 2 of 7 reported patients
- Bulbous noseHPOHP:0000414
- 1 of 5 reported patients
- EntropionHPOHP:0000621
- 1 of 5 reported patients
- Highly arched eyebrowHPOHP:0002553
- 1 of 5 reported patients
- Hypoplastic superior helixHPOHP:0008559
- 1 of 5 reported patients
- Long eyelashesHPOHP:0000527
- 1 of 5 reported patients
Where it sits
- A kind of