macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome
MONDO:0014757Mondo
Findings
No curated finding names macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
74 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.
- CamptodactylyHPOHP:0012385
- 2 of 2 reported patients · Childhood onset
- Occasional (5% to 29% of cases)
- Dental malocclusionHPOHP:0000689
- 2 of 2 reported patients · Childhood onset
- Occasional (5% to 29% of cases)
- Eversion of lateral third of lower eyelidsHPOHP:0007655
- 2 of 2 reported patients
- Occasional (5% to 29% of cases)
- ExotropiaHPOHP:0000577
- 2 of 2 reported patients · Childhood onset
- Occasional (5% to 29% of cases)
- Global developmental delayHPOHP:0001263
- 2 of 2 reported patients
- Occasional (5% to 29% of cases)
- Highly arched eyebrowHPOHP:0002553
- 2 of 2 reported patients
- Occasional (5% to 29% of cases)
- Increased mean platelet volumeHPOHP:0011877
- 2 of 2 reported patients
- Frequent (30% to 79% of cases)
- LymphedemaHPOHP:0001004
- 2 of 2 reported patients · Childhood onset
- Occasional (5% to 29% of cases)
- Midface retrusionHPOHP:0011800
- 2 of 2 reported patients · Childhood onset
- Occasional (5% to 29% of cases)
- Progressive microcephalyHPOHP:0000253
- 2 of 2 reported patients · Childhood onset
- PtosisHPOHP:0000508
- 2 of 2 reported patients
- Occasional (5% to 29% of cases)
- Sensorineural hearing impairmentHPOHP:0000407
- 2 of 2 reported patients · Childhood onset
Show the remaining 62
- Short philtrumHPOHP:0000322
- 2 of 2 reported patients · Childhood onset
- Occasional (5% to 29% of cases)
- Thin upper lip vermilionHPOHP:0000219
- 2 of 2 reported patients · Childhood onset
- Occasional (5% to 29% of cases)
- VentriculomegalyHPOHP:0002119
- 2 of 2 reported patients
- Frequent (30% to 79% of cases)
- Abnormal facial shapeHPOHP:0001999
- Very frequent (80% to 99% of cases)
- Brain imaging abnormalityHPOHP:0410263
- Very frequent (80% to 99% of cases)
- Abnormal heart morphologyHPO
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.
- CDC42HGNC:1736
- Definitive · ClinGen · Autosomal dominant · 2021
- Definitive · G2P · Autosomal dominant · 2025
- Strong · Ambry Genetics · Autosomal dominant · 2018
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2022
Where it sits
Other names
1 name
Resolves to: macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome
- Also called
- Takenouchi-Kosaki syndrome