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1 OMIM reference -
1 associated gene
8 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 2
1 OMIM reference -
1 associated gene
10 signs/symptoms
Stickler syndrome type 2
Multiple epiphyseal dysplasia, Beighton type

COL11A1 COL2A1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
COL11A1
(0.52)
COL2A1



Citations in the biomedical literature:


Stickler syndrome type 2
COL11A1
Multiple epiphyseal dysplasia, Beighton type
COL2A1



Stickler syndrome type 2
Multiple epiphyseal dysplasia, Beighton type

Synonym(s):
(no synonyms)

Synonym(s):
- Multiple epiphyseal dysplasia - myopia - deafness

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare maxillo-facial surgical disease
- Rare otorhinolaryngologic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: C537493
External references:
1 OMIM reference -
No MeSH references


COMMON
SIGNS
- Cataract / lens opacification
- Myopia


Stickler syndrome type 2
Multiple epiphyseal dysplasia, Beighton type

Very frequent
- Corneal clouding / opacity / vascularisation
- Retinal detachment
- Sensorineural deafness / hearing loss
- Vitreous anomalies / hyalitis / persistent vitreous vascularisation

Frequent
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Retinopathy



Very frequent
- Absent / small fingernails / anonychia of hands
- Autosomal dominant inheritance
- Conductive deafness / hearing loss
- Epiphyseal anomaly
- Flat face
- Microstomia / little mouth
- Round face
- Short hand / brachydactyly