intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies
MONDO:0032832Mondo
Findings
No curated finding names intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies 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
20 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
- 3 of 3 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 4 of 4 reported patients
- Feeding difficulties in infancyHPOHP:0008872
- 4 of 4 reported patients · Infantile onset
- Generalized hypotoniaHPOHP:0001290
- 4 of 4 reported patients
- Long eyelashesHPOHP:0000527
- 2 of 2 reported patients
- Low-set earsHPOHP:0000369
- 4 of 4 reported patients
- MicrognathiaHPOHP:0000347
- 4 of 4 reported patients
- Thin upper lip vermilionHPOHP:0000219
- 3 of 3 reported patients
- Upslanted palpebral fissureHPOHP:0000582
- 3 of 3 reported patients
- Hypernasal speechHPOHP:0001611
- 3 of 4 reported patients
- Thick eyebrowHPOHP:0000574
- 2 of 3 reported patients
- HirsutismHPOHP:0001007
- 2 of 4 reported patients
Show the remaining 8
- Short 5th fingerHPOHP:0009237
- 2 of 4 reported patients
- Horizontal eyebrowHPOHP:0011228
- 1 of 3 reported patients
- 2-3 toe syndactylyHPOHP:0004691
- 1 of 4 reported patients
- Clinodactyly of the 5th fingerHPOHP:0004209
- 1 of 4 reported patients
- Hearing impairmentHPOHP:0000365
- 1 of 4 reported patients
- ScoliosisHPOHP:0002650
- 1 of 4 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- CNOT2HGNC:7878
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2022
- Strong · G2P · Autosomal dominant · 2025
Where it sits
- A kind of