neurodevelopmental disorder with neuromuscular and skeletal abnormalities
MONDO:0859236Mondo
Findings
No curated finding names neurodevelopmental disorder with neuromuscular and skeletal abnormalities 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 · Juvenile onset · Early young adult onset
HPO, annotations 2026-09-02
Features
58 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.
- ScoliosisHPOHP:0002650
- 5 of 9 reported patients
- MicrocephalyHPOHP:0000252
- 3 of 6 reported patients
- Global developmental delayHPOHP:0001263
- 4 of 10 reported patients
- HypotoniaHPOHP:0001252
- 4 of 10 reported patients
- IrritabilityHPOHP:0000737
- 2 of 5 reported patients
- Self-injurious behaviorHPOHP:0100716
- 2 of 5 reported patients
- MicrognathiaHPOHP:0000347
- 3 of 8 reported patients
- Hip dysplasiaHPOHP:0001385
- 3 of 9 reported patients
- Pes cavusHPOHP:0001761
- 3 of 9 reported patients
- Cerebral palsyHPOHP:0100021
- 3 of 10 reported patients
- Intellectual disabilityHPOHP:0001249
- 3 of 10 reported patients
- Motor delayHPOHP:0001270
- 3 of 10 reported patients
Show the remaining 46
- CataractHPOHP:0000518
- 2 of 8 reported patients
- Depressed nasal bridgeHPOHP:0005280
- 2 of 8 reported patients
- Failure to thriveHPOHP:0001508
- 2 of 8 reported patients
- Short statureHPOHP:0004322
- 2 of 8 reported patients
- StrabismusHPOHP:0000486
- 2 of 8 reported patients
- Tented upper lip vermilionHPOHP:0010804
- 2 of 8 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.
- NRCAMHGNC:7994
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · Ambry Genetics · Autosomal recessive · 2022
- Moderate · G2P · Autosomal recessive · 2022