macrocephaly/megalencephaly syndrome, autosomal recessive
MONDO:0009544Mondo
Findings
No curated finding names macrocephaly/megalencephaly syndrome, 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
- Infantile onset
HPO, annotations 2026-09-02
Features
16 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.
- Broad foreheadHPOHP:0000337
- 2 of 2 reported patients
- Calcium oxalate nephrolithiasisHPOHP:0008672
- 2 of 2 reported patients
- Celiac diseaseHPOHP:0002608
- 2 of 2 reported patients
- DolichocephalyHPOHP:0000268
- 2 of 2 reported patients
- MacrocephalyHPOHP:0000256
- 4 of 4 reported patients
- Mild intellectual disabilityHPOHP:0001256
- 4 of 4 reported patients
- MyopiaHPOHP:0000545
- 2 of 2 reported patients
- Patellar subluxationHPOHP:0010499
- 2 of 2 reported patients
- Pointed chinHPOHP:0000307
- 2 of 2 reported patients
- PsychosisHPOHP:0000709
- 2 of 2 reported patients
- Thick corpus callosumHPOHP:0007074
- 2 of 2 reported patients
- ScaphocephalyHPOHP:0030799
- 3 of 4 reported patients
Show the remaining 4
- Genu valgumHPOHP:0002857
- 1 of 2 reported patients
- StrabismusHPOHP:0000486
- 1 of 2 reported patients
- HydrocephalusHPOHP:0000238
- 0 of 2 reported patients
- MegalencephalyHPOHP:0001355
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.
- TBC1D7HGNC:21066
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2018
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · Genomics England PanelApp · Autosomal recessive · 2021
- Limited · Ambry Genetics · Autosomal recessive · 2018