microcephaly-micromelia syndrome
MONDO:0009619Mondo
Findings
No curated finding names microcephaly-micromelia 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 · Neonatal death
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.
- MicrocephalyHPOHP:0000252
- 2 of 2 reported patients · Antenatal onset
- Absent thumbHPOHP:0009777
- Aplasia/Hypoplasia of the corpus callosumHPOHP:0007370
- Aqueductal stenosisHPOHP:0002410
- Convex nasal ridgeHPOHP:0000444
- CraniosynostosisHPOHP:0001363
- Forearm undergrowthHPOHP:0009821
- Intrauterine growth retardationHPOHP:0001511
- Low-set earsHPOHP:0000369
- MicrognathiaHPOHP:0000347
- MicromeliaHPOHP:0002983
- Missing ribsHPOHP:0000921
Show the remaining 7
- Narrow mouthHPOHP:0000160
- OligodactylyHPOHP:0012165
- Short neckHPOHP:0000470
- Short palpebral fissureHPOHP:0012745
- Simplified gyral patternHPOHP:0009879
- Talipes equinovarusHPOHP:0001762
- Wide noseHPOHP:0000445
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.
- DONSONHGNC:2993
- Strong · PanelApp Australia · Autosomal recessive · 2025
Where it sits
- A kind of