microcephaly 5, primary, autosomal recessive
Findings
No curated finding names microcephaly 5, primary, autosomal recessive yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the ASPM gene.
Definition from the Mondo Disease Ontology (MONDO:0012106), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Congenital onset · Fetal 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.
- Delayed speech and language developmentHPOHP:0000750
- 1 of 1 reported patient
- EpicanthusHPOHP:0000286
- 1 of 1 reported patient
- High palateHPOHP:0000218
- 1 of 1 reported patient
- Intellectual disabilityHPOHP:0001249
- 24 of 24 reported patients
- Lateral ventricle dilatationHPOHP:0006956
- 1 of 1 reported patient
- MicrocephalyHPOHP:0000252
- 28 of 28 reported patients
- MicrognathiaHPOHP:0000347
Show the remaining 7
- Short statureHPOHP:0004322
- 16 of 22 reported patients
- Decreased body weightHPOHP:0004325
- 14 of 22 reported patients
- HyperactivityHPOHP:0000752
- 7 of 20 reported patients
- Flat occiputHPOHP:0005469
- 1 of 6 reported patients
- Aggressive behaviorHPOHP:0000718
- 3 of 21 reported patients
- Self-injurious behaviorHPOHP:0100716
- 2 of 21 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.
- ASPMHGNC:19048
- Definitive · G2P · Autosomal recessive · 2025
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
- Strong · PanelApp Australia · Autosomal recessive · 2025
Where it sits
Other names
2 names
Resolves to: microcephaly 5, primary, autosomal recessive
- Also called
- ASPM autosomal recessive primary microcephalyautosomal recessive primary microcephaly caused by mutation in ASPM