microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome
MONDO:0020647Mondo
Findings
No curated finding names microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome 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
20 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
- 3 of 3 reported patients
- MicrognathiaHPOHP:0000347
- 3 of 3 reported patients
- Unilateral renal agenesisHPOHP:0000122
- 3 of 3 reported patients
- Intrauterine growth retardationHPOHP:0001511
- 2 of 3 reported patients
- Agenesis of corpus callosumHPOHP:0001274
- 1 of 3 reported patients
- Ambiguous genitaliaHPOHP:0000062
- 1 of 3 reported patients
- Bilateral talipes equinovarusHPOHP:0001776
- 1 of 3 reported patients
- BrachycephalyHPOHP:0000248
- 1 of 3 reported patients
- Crossed fused renal ectopiaHPOHP:0004736
- 1 of 3 reported patients
- Enlarged cisterna magnaHPOHP:0002280
- 1 of 3 reported patients
- Hypoplasia of the corpus callosumHPOHP:0002079
- 1 of 3 reported patients
- Hypoplastic right ventricleHPOHP:0010954
- 1 of 3 reported patients
Show the remaining 8
- LissencephalyHPOHP:0001339
- 1 of 3 reported patients
- Low-set earsHPOHP:0000369
- 1 of 3 reported patients
- MacrotiaHPOHP:0000400
- 1 of 3 reported patients
- MicropenisHPOHP:0000054
- 1 of 3 reported patients
- Overlapping toeHPOHP:0001845
- 1 of 3 reported patients
- Preaxial polydactylyHPOHP:0100258
- 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.
- CTU2HGNC:28005
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2020
- Strong · G2P · Autosomal recessive · 2019
- Limited · Ambry Genetics · Autosomal recessive · 2018
Where it sits
- A kind of
Other names
1 name
Resolves to: microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome
- Also called
- MFRG