neurofacioskeletal syndrome with or without renal agenesis
MONDO:0030966Mondo
Findings
No curated finding names neurofacioskeletal syndrome with or without renal agenesis 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
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.
- Delayed speech and language developmentHPOHP:0000750
- 2 of 2 reported patients
- Global developmental delayHPOHP:0001263
- 2 of 2 reported patients
- Intellectual disabilityHPOHP:0001249
- 2 of 2 reported patients
- MicrodontiaHPOHP:0000691
- 1 of 1 reported patient
- Motor delayHPOHP:0001270
- 2 of 2 reported patients
- Coarse facial featuresHPOHP:0000280
- 3 of 4 reported patients
- Elbow flexion contractureHPOHP:0002987
- 3 of 4 reported patients
- Hip contractureHPOHP:0003273
- 3 of 4 reported patients
- Low-set earsHPOHP:0000369
- 3 of 4 reported patients
- Upslanted palpebral fissureHPOHP:0000582
- 3 of 4 reported patients
- Wide mouthHPOHP:0000154
- 3 of 4 reported patients
- Feeding difficultiesHPOHP:0011968
- 2 of 3 reported patients
Show the remaining 46
- Broad distal phalanx of fingerHPOHP:0009836
- 2 of 4 reported patients
- Broad distal phalanx of the toesHPOHP:0010186
- 2 of 4 reported patients
- Broad nasal tipHPOHP:0000455
- 2 of 4 reported patients
- CryptorchidismHPOHP:0000028
- 1 of 2 reported patients
- Deep philtrumHPOHP:0002002
- 2 of 4 reported patients
- Hypoplasia of the capital femoral epiphysisHPOHP:0003090
- 2 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.
- HS2ST1HGNC:5193
- Strong · G2P · Autosomal recessive · 2025
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2021
Where it sits
- A kind of
Other names
2 names
Resolves to: neurofacioskeletal syndrome with or without renal agenesis
- Also called
- Neurodevelopmental Disorder With Corpus Callosum Agenesis, Craniofacial Dysmorphism, and Skeletal Anomalies, With or Without Renal AgenesisNFSRA