neurodevelopmental disorder with poor growth and skeletal anomalies
MONDO:0859252Mondo
Findings
No curated finding names neurodevelopmental disorder with poor growth and skeletal anomalies yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Congenital onset · Infantile onset · Neonatal onset
HPO, annotations 2026-09-02
Features
29 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.
- Intellectual disabilityHPOHP:0001249
- 18 of 19 reported patients
- MicrocephalyHPOHP:0000252
- 12 of 19 reported patients
- HypotoniaHPOHP:0001252
- 10 of 19 reported patients
- SeizureHPOHP:0001250
- 10 of 19 reported patients
- Prominent nasal bridgeHPOHP:0000426
- 7 of 19 reported patients
- Broad thumbHPOHP:0011304
- 3 of 19 reported patients
- Cerebral cortical atrophyHPOHP:0002120
- 3 of 19 reported patients
- ClinodactylyHPOHP:0030084
- 3 of 19 reported patients
- High, narrow palateHPOHP:0002705
- 3 of 19 reported patients
- Metopic synostosisHPOHP:0011330
- 3 of 19 reported patients
- Swan neck-like deformities of the fingersHPOHP:0006150
- 3 of 19 reported patients
- SynophrysHPOHP:0000664
- 3 of 19 reported patients
Show the remaining 17
- Ulnar deviated club handsHPOHP:0006055
- 3 of 19 reported patients
- EpicanthusHPOHP:0000286
- 2 of 19 reported patients
- EsotropiaHPOHP:0000565
- 2 of 19 reported patients
- Everted lower lip vermilionHPOHP:0000232
- 2 of 19 reported patients
- Long faceHPOHP:0000276
- 2 of 19 reported patients
- Mandibular prognathiaHPOHP:0000303
- 2 of 19 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.
- HGNC:8717HGNC:8717
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2022
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Strong · G2P · Autosomal recessive · 2021