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13 OMIM references -
10 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
4 OMIM references -
4 associated genes
4 signs/symptoms
Nuclear cataract
Microphthalmia - cataract

CRYAA CRYBA4
CRYBB1 SIX6
CRYBB2 TMEM114
CRYBB3 VSX2
CRYGD
FYCO1
GJA3
MIP
NHS
WFS1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CRYBB1
CRYBB2
(0.63)
(0.63)
CRYBA4
CRYBA4



Citations in the biomedical literature:


Nuclear cataract
CRYAA CRYBB1 CRYBB2 CRYBB3 CRYGD FYCO1
GJA3 MIP NHS WFS1
Microphthalmia - cataract
CRYBA4 SIX6 TMEM114 VSX2



Nuclear cataract
Microphthalmia - cataract

Synonym(s):
(no synonyms)

Synonym(s):
- Congenital cataract - microphthalmia

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- 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: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
13 OMIM references -
No MeSH references
External references:
4 OMIM references -
No MeSH references

Microphthalmia - cataract

Frequent
- Anophthalmos / anophthalmia / microphthalmos / microphthalmia
- Autosomal dominant inheritance
- Coloboma of iris
- Retinoschisis / retinal / chorioretinal coloboma



Nuclear cataract

(no data available)