Seckel syndrome 11
MONDO:0958328Mondo
Findings
No curated finding names Seckel syndrome 11 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
HPO, annotations 2026-09-02
Features
35 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.
- ClinodactylyHPOHP:0030084
- 4 of 4 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 2 of 2 reported patients
- Global developmental delayHPOHP:0001263
- 2 of 2 reported patients
- Highly arched eyebrowHPOHP:0002553
- 4 of 4 reported patients
- Intellectual disabilityHPOHP:0001249
- 2 of 2 reported patients
- Long philtrumHPOHP:0000343
- 4 of 4 reported patients
- Motor delayHPOHP:0001270
- 2 of 2 reported patients
- Primary microcephalyHPOHP:0011451
- 4 of 4 reported patients
- Prominent nasal bridgeHPOHP:0000426
- 4 of 4 reported patients
- Protruding earHPOHP:0000411
- 4 of 4 reported patients
- Simplified gyral patternHPOHP:0009879
- 3 of 3 reported patients
- Smooth philtrumHPOHP:0000319
- 4 of 4 reported patients
Show the remaining 23
- Thin upper lip vermilionHPOHP:0000219
- 4 of 4 reported patients
- Broad 2nd toeHPOHP:0100040
- 3 of 4 reported patients
- Feeding difficultiesHPOHP:0011968
- 3 of 4 reported patients
- Postnatal growth retardationHPOHP:0008897
- 3 of 4 reported patients
- Short statureHPOHP:0004322
- 3 of 4 reported patients
- PachygyriaHPOHP:0001302
- 2 of 3 reported patients
Where it sits
- A kind of