microcephaly 15, primary, autosomal recessive
MONDO:0014660Mondo
Findings
No curated finding names microcephaly 15, primary, autosomal recessive 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 · Death in childhood · Death in adolescence
HPO, annotations 2026-09-02
Features
15 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 speechHPOHP:0001344
- 3 of 3 reported patients
- HyperreflexiaHPOHP:0001347
- 3 of 3 reported patients
- Hypoplasia of the corpus callosumHPOHP:0002079
- 3 of 3 reported patients
- HypotoniaHPOHP:0001252
- 3 of 3 reported patients
- Inability to walkHPOHP:0002540
- 3 of 3 reported patients
- MicrocephalyHPOHP:0000252
- 3 of 3 reported patients
- Poor head controlHPOHP:0002421
- 3 of 3 reported patients
- Severe intellectual disabilityHPOHP:0010864
- 3 of 3 reported patients
- Spastic tetraparesisHPOHP:0001285
- 3 of 3 reported patients
- VentriculomegalyHPOHP:0002119
- 3 of 3 reported patients
- Autistic behaviorHPOHP:0000729
- 2 of 3 reported patients
- Bilateral talipes equinovarusHPOHP:0001776
- 2 of 3 reported patients
Show the remaining 3
- AtaxiaHPOHP:0001251
- 0 of 3 reported patients
- Upslanted palpebral fissureHPOHP:0000582
- 0 of 3 reported patients
- Global developmental delayHPOHP:0001263
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.
- MFSD2AHGNC:25897
- Definitive · G2P · Autosomal recessive · 2016
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2021
- Strong · PanelApp Australia · Autosomal recessive · 2025
Where it sits
Other names
1 name
Resolves to: microcephaly 15, primary, autosomal recessive
- Also called
- neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities