vertebral, cardiac, renal, and limb defects syndrome 1
MONDO:0060554Mondo
Findings
No curated finding names vertebral, cardiac, renal, and limb defects syndrome 1 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
19 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.
- MicrocephalyHPOHP:0000252
- 2 of 2 reported patients
- Renal hypoplasiaHPOHP:0000089
- 2 of 2 reported patients
- Sensorineural hearing impairmentHPOHP:0000407
- 2 of 2 reported patients
- Atrial septal defectHPOHP:0001631
- 1 of 2 reported patients
- Bifid uvulaHPOHP:0000193
- 1 of 2 reported patients
- Butterfly vertebraeHPOHP:0003316
- 1 of 2 reported patients
- Global developmental delayHPOHP:0001263
- 1 of 2 reported patients
- Hypoplastic left ventricleHPOHP:0004383
- 1 of 2 reported patients
- Incomplete partition of the cochlea type IIHPOHP:0000376
- 1 of 2 reported patients
- Intellectual disabilityHPOHP:0001249
- 1 of 2 reported patients
- Laryngeal webHPOHP:0005950
- 1 of 2 reported patients
- LaryngomalaciaHPOHP:0001601
- 1 of 2 reported patients
Show the remaining 7
- Short statureHPOHP:0004322
- 1 of 2 reported patients
- Spinal dysraphismHPOHP:0010301
- 1 of 2 reported patients
- Submucous cleft hard palateHPOHP:0000176
- 1 of 2 reported patients
- TalipesHPOHP:0001883
- 1 of 2 reported patients
- Tethered cordHPOHP:0002144
- 1 of 2 reported patients
- Unilateral vocal cord paresisHPOHP:0012821
- 1 of 2 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.
- HAAOHGNC:4796
- Definitive · ClinGen · Autosomal recessive · 2022
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2018
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · G2P · Autosomal recessive · 2022
- Limited · Ambry Genetics · Autosomal recessive · 2018