Tayoun-Maawali syndrome
MONDO:0976286Mondo
Findings
No curated finding names Tayoun-Maawali syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Congenital onset · Antenatal onset
HPO, annotations 2026-09-02
Features
116 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.
- Bilateral tonic-clonic seizureHPOHP:0002069
- 1 of 1 reported patient
- Biventricular hypertrophyHPOHP:0200128
- 1 of 1 reported patient
- Coarctation of aortaHPOHP:0001680
- 1 of 1 reported patient
- Failure to thriveHPOHP:0001508
- 13 of 13 reported patients
- Neurodevelopmental delayHPOHP:0012758
- 13 of 14 reported patients
- Abnormal facial shapeHPOHP:0001999
- 9 of 10 reported patients
- Poor suckHPOHP:0002033
- 6 of 7 reported patients
- Small for gestational ageHPOHP:0001518
- 5 of 6 reported patients
- Hyperechogenic kidneysHPOHP:0004719
- 3 of 4 reported patients
- MicropenisHPOHP:0000054
- 3 of 4 reported patients
- Primary microcephalyHPOHP:0011451
- 3 of 4 reported patients
- Intrauterine growth retardationHPOHP:0001511
- 11 of 15 reported patients
Show the remaining 104
- Generalized hypotoniaHPOHP:0001290
- 8 of 12 reported patients
- MicrocephalyHPOHP:0000252
- 8 of 12 reported patients
- Renal hypoplasiaHPOHP:0000089
- 2 of 3 reported patients
- Short statureHPOHP:0004322
- 10 of 15 reported patients
- Depressed nasal bridgeHPOHP:0005280
- 9 of 14 reported patients
- High foreheadHPOHP:0000348
- 8 of 14 reported patients
Where it sits
- A kind of