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13 OMIM references -
10 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
4 OMIM references -
3 associated genes
No signs/symptoms info
Nuclear cataract
Male infertility with normal virilization due to meiosis defect

CRYAA CFTR
CRYBB1 SOHLH1
CRYBB2 SYCP3
CRYBB3
CRYGD
FYCO1
GJA3
MIP
NHS
WFS1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
WFS1
NHS
(0.63)
(0.56)
CFTR
CFTR



Citations in the biomedical literature:


Nuclear cataract
CRYAA CRYBB1 CRYBB2 CRYBB3 CRYGD FYCO1
GJA3 MIP NHS WFS1
Male infertility with normal virilization due to meiosis defect
CFTR SOHLH1 SYCP3



Nuclear cataract
Male infertility with normal virilization due to meiosis defect

Synonym(s):
(no synonyms)

Synonym(s):
- Azoospermia due to maturation arrest
- Azoospermia due to meiosis defect
- Male infertility with normal virilization due to maturation arrest

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: -
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: -
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.