Harel-Tora neurodevelopmental syndrome
MONDO:0980703Mondo
Findings
No curated finding names Harel-Tora neurodevelopmental syndrome 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
84 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.
- AtaxiaHPOHP:0001251
- 2 of 2 reported patients
- Broad halluxHPOHP:0010055
- 1 of 1 reported patient
- ChilblainsHPOHP:0009710
- 1 of 1 reported patient
- Delayed ability to walkHPOHP:0031936
- 7 of 7 reported patients
- DroolingHPOHP:0002307
- 1 of 1 reported patient
- EpistaxisHPOHP:0000421
- 1 of 1 reported patient
- Expressive language delayHPOHP:0002474
- 2 of 2 reported patients
- Feeding difficultiesHPOHP:0011968
- 1 of 1 reported patient
- Flat faceHPOHP:0012368
- 1 of 1 reported patient
- Frequent fallsHPOHP:0002359
- 1 of 1 reported patient
- Gait imbalanceHPOHP:0002141
- 1 of 1 reported patient
- Gastroesophageal refluxHPOHP:0002020
- 2 of 2 reported patients
Show the remaining 72
- HyperreflexiaHPOHP:0001347
- 1 of 1 reported patient
- Inability to walkHPOHP:0002540
- 2 of 2 reported patients
- Inverted nipplesHPOHP:0003186
- 1 of 1 reported patient
- Long fingersHPOHP:0100807
- 2 of 2 reported patients
- Low anterior hairlineHPOHP:0000294
- 1 of 1 reported patient
- Moderate intellectual disabilityHPOHP:0002342
- 3 of 3 reported patients