robinow syndrome, autosomal recessive 2
MONDO:0032800Mondo
Findings
No curated finding names robinow syndrome, autosomal recessive 2 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
34 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
- BrachydactylyHPOHP:0001156
- 3 of 3 reported patients
- Broad halluxHPOHP:0010055
- 3 of 3 reported patients
- Broad thumbHPOHP:0011304
- 3 of 3 reported patients
- ClinodactylyHPOHP:0030084
- 3 of 3 reported patients
- Gingival overgrowthHPOHP:0000212
- 3 of 3 reported patients
- High foreheadHPOHP:0000348
- 3 of 3 reported patients
- HypertelorismHPOHP:0000316
- 3 of 3 reported patients
- Long philtrumHPOHP:0000343
- 3 of 3 reported patients
- MesomeliaHPOHP:0003027
- 3 of 3 reported patients
- MicrognathiaHPOHP:0000347
- 3 of 3 reported patients
- ProptosisHPOHP:0000520
- 3 of 3 reported patients
Show the remaining 22
- Triangular mouthHPOHP:0000207
- 3 of 3 reported patients
- Absent uvulaHPOHP:0010292
- 2 of 3 reported patients
- CamptodactylyHPOHP:0012385
- 2 of 3 reported patients
- Frontal bossingHPOHP:0002007
- 2 of 3 reported patients
- Midface retrusionHPOHP:0011800
- 2 of 3 reported patients
- Prominent fingertip padsHPOHP:0001212
- 2 of 3 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.
- NXNHGNC:18008
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2019
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · Ambry Genetics · Autosomal recessive · 2024
Where it sits
- A kind of