neurodevelopmental disorder with dysmorphic facies and distal limb anomalies
MONDO:0060596Mondo
Findings
No curated finding names neurodevelopmental disorder with dysmorphic facies and distal limb 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
27 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.
- Delayed speech and language developmentHPOHP:0000750
- 10 of 10 reported patients
- Global developmental delayHPOHP:0001263
- 10 of 10 reported patients
- Motor delayHPOHP:0001270
- 8 of 10 reported patients
- MicrocephalyHPOHP:0000252
- 7 of 9 reported patients
- Prominent noseHPOHP:0000448
- 7 of 10 reported patients
- Broad halluxHPOHP:0010055
- 5 of 10 reported patients
- Generalized hypotoniaHPOHP:0001290
- 5 of 10 reported patients
- Short statureHPOHP:0004322
- 4 of 10 reported patients
- Abnormal cerebral white matter morphologyHPOHP:0002500
- 3 of 10 reported patients
- Clinodactyly of the 5th fingerHPOHP:0004209
- 3 of 10 reported patients
- MicrognathiaHPOHP:0000347
- 3 of 10 reported patients
- Broad eyebrowHPOHP:0011229
- 2 of 10 reported patients
Show the remaining 15
- HypertelorismHPOHP:0000316
- 2 of 10 reported patients
- Long nasal bridgeHPOHP:0033142
- 2 of 10 reported patients
- Short palpebral fissureHPOHP:0012745
- 2 of 10 reported patients
- Upslanted palpebral fissureHPOHP:0000582
- 2 of 10 reported patients
- Broad nasal tipHPOHP:0000455
- 1 of 10 reported patients
- EpicanthusHPOHP:0000286
- 1 of 10 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.
- BPTFHGNC:3581
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2022
- Strong · G2P · Autosomal dominant · 2025
- Strong · PanelApp Australia · Autosomal dominant · 2025