skin creases, congenital symmetric circumferential, 2
MONDO:0014755Mondo
Findings
No curated finding names skin creases, congenital symmetric circumferential, 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Congenital onset
HPO, annotations 2026-09-02
Features
39 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.
- Circumferential skin creases on extremitiesHPOHP:0034400
- 4 of 4 reported patients
- Hypoplasia of the corpus callosumHPOHP:0002079
- 2 of 2 reported patients
- Intellectual disabilityHPOHP:0001249
- 4 of 4 reported patients
- MicrophthalmiaHPOHP:0000568
- 4 of 4 reported patients
- VentriculomegalyHPOHP:0002119
- 2 of 2 reported patients
- Wide nasal bridgeHPOHP:0000431
- 4 of 4 reported patients
- Cleft palateHPOHP:0000175
- 3 of 4 reported patients
- Low-set earsHPOHP:0000369
- 3 of 4 reported patients
- Short palpebral fissureHPOHP:0012745
- 3 of 4 reported patients
- EpicanthusHPOHP:0000286
- 2 of 4 reported patients
- Flat faceHPOHP:0012368
- 2 of 4 reported patients
- Overfolded helixHPOHP:0000396
- 2 of 4 reported patients
Show the remaining 27
- Posteriorly rotated earsHPOHP:0000358
- 2 of 4 reported patients
- SeizureHPOHP:0001250
- 2 of 4 reported patients
- Upslanted palpebral fissureHPOHP:0000582
- 2 of 4 reported patients
- 2-3 toe syndactylyHPOHP:0004691
- 1 of 4 reported patients
- Clinodactyly of the 5th fingerHPOHP:0004209
- 1 of 4 reported patients
- Depressed nasal bridgeHPOHP:0005280
- 1 of 4 reported patients
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.
- MAPRE2HGNC:6891
- Definitive · G2P · Autosomal recessive · 2016
- Strong · PanelApp Australia · Semidominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2020
- Moderate · G2P · Autosomal dominant · 2025
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2021
Where it sits
Other names
6 names
Resolves to: skin creases, congenital symmetric circumferential, 2
- Also called
- CSCSC2MAPRE2 multiple benign circumferential skin creases on limbsmultiple benign circumferential skin creases on limbs caused by mutation in MAPRE2skin creases, congenital symmetric circumferential, 2; CSCSC2skin creases, congenital symmetric circumferential, type 2symmetric circumferential skin creases, congenital, 2