tetraamelia syndrome 1
MONDO:0060764Mondo
Findings
No curated finding names tetraamelia 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
- Fetal onset
HPO, annotations 2026-09-02
Features
21 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.
- Absent external genitaliaHPOHP:0000042
- 1 of 1 reported patient
- TetraameliaHPOHP:0003057
- 4 of 4 reported patients
- Cleft palateHPOHP:0000175
- 2 of 3 reported patients
- Cleft upper lipHPOHP:0000204
- 2 of 3 reported patients
- Hypoplastic pelvisHPOHP:0008839
- 2 of 3 reported patients
- Renal agenesisHPOHP:0000104
- 2 of 3 reported patients
- Hypoplasia of the fallopian tubeHPOHP:0008697
- 1 of 2 reported patients
- Vaginal atresiaHPOHP:0000148
- 1 of 2 reported patients
- Adrenal gland agenesisHPOHP:0011743
- 1 of 3 reported patients
- Anal atresiaHPOHP:0002023
- 1 of 3 reported patients
- AspleniaHPOHP:0001746
- 1 of 3 reported patients
- CataractHPOHP:0000518
- 1 of 3 reported patients
Show the remaining 9
- Choanal atresiaHPOHP:0000453
- 1 of 3 reported patients
- Congenital diaphragmatic herniaHPOHP:0000776
- 1 of 3 reported patients
- GastroschisisHPOHP:0001543
- 1 of 3 reported patients
- MicrophthalmiaHPOHP:0000568
- 1 of 3 reported patients
- Single narisHPOHP:0009932
- 1 of 3 reported patients
- Single umbilical arteryHPOHP:0001195
- 1 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.
- WNT3HGNC:12782
- Definitive · G2P · Autosomal recessive · 2017
- Moderate · Genomics England PanelApp · Autosomal recessive · 2021
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2019
- Limited · PanelApp Australia · Autosomal recessive · 2025
- Limited · ClinGen · Autosomal recessive · 2026