Menke-Hennekam syndrome 2
MONDO:0020769Mondo
Findings
No curated finding names Menke-Hennekam syndrome 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
28 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.
- Agenesis of permanent teethHPOHP:0006349
- 2 of 2 reported patients
- Autistic behaviorHPOHP:0000729
- 2 of 2 reported patients
- Delayed ability to walkHPOHP:0031936
- 1 of 1 reported patient
- Delayed speech and language developmentHPOHP:0000750
- 1 of 1 reported patient
- Depressed nasal bridgeHPOHP:0005280
- 2 of 2 reported patients
- Flat faceHPOHP:0012368
- 2 of 2 reported patients
- Recurrent upper respiratory tract infectionsHPOHP:0002788
- 2 of 2 reported patients
- Short palpebral fissureHPOHP:0012745
- 2 of 2 reported patients
- Thin upper lip vermilionHPOHP:0000219
- 2 of 2 reported patients
- Upslanted palpebral fissureHPOHP:0000582
- 2 of 2 reported patients
- Absent earlobeHPOHP:0000387
- 1 of 2 reported patients
- BlepharophimosisHPOHP:0000581
- 1 of 2 reported patients
Show the remaining 16
- Chronic constipationHPOHP:0012450
- 1 of 2 reported patients
- Cutaneous syndactyly of toesHPOHP:0010621
- 1 of 2 reported patients
- Deep philtrumHPOHP:0002002
- 1 of 2 reported patients
- Duodenal ulcerHPOHP:0002588
- 1 of 2 reported patients
- EpicanthusHPOHP:0000286
- 1 of 2 reported patients
- Full cheeksHPOHP:0000293
- 1 of 2 reported patients
Where it sits
- A kind of