gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy
MONDO:0032738Mondo
Findings
No curated finding names gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy 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
45 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.
- Clitoral hypoplasiaHPOHP:0000060
- 4 of 4 reported patients
- Convex nasal ridgeHPOHP:0000444
- 4 of 4 reported patients
- Cutaneous finger syndactylyHPOHP:0010554
- 4 of 4 reported patients
- Delayed skeletal maturationHPOHP:0002750
- 4 of 4 reported patients
- Dry skinHPOHP:0000958
- 4 of 4 reported patients
- EpicanthusHPOHP:0000286
- 4 of 4 reported patients
- Flat faceHPOHP:0012368
- 4 of 4 reported patients
- Frontal upsweep of hairHPOHP:0002236
- 4 of 4 reported patients
- Gonadal dysgenesisHPOHP:0000133
- 4 of 4 reported patients
- Highly arched eyebrowHPOHP:0002553
- 4 of 4 reported patients
- HypodontiaHPOHP:0000668
- 4 of 4 reported patients
- Hypoplasia of the lacrimal punctumHPOHP:0007892
- 4 of 4 reported patients
Show the remaining 33
- Hypoplasia of the uterusHPOHP:0000013
- 4 of 4 reported patients
- Hypoplastic labia majoraHPOHP:0000059
- 4 of 4 reported patients
- Limited elbow extensionHPOHP:0001377
- 4 of 4 reported patients
- Long philtrumHPOHP:0000343
- 4 of 4 reported patients
- Low-set earsHPOHP:0000369
- 4 of 4 reported patients
- Overfolded helixHPOHP:0000396
- 4 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.
- PPP2R3CHGNC:17485
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2022
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Limited · Ambry Genetics · Autosomal recessive · 2022
Where it sits
- A kind of
Other names
3 names
Resolves to: gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy
- Also called
- agonadism, 46,XY, with intellectual disability, short stature, retarded bone age, and multiple extragenital malformationsagonadism, 46,XY, with mental retardation, short stature, retarded bone age, and multiple extragenital malformationsKENNERKNECHT syndrome