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Zonular cataract
9 OMIM references -
9 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 5
Fatal infantile hypertonic myofibrillar myopathy
1 OMIM reference -
1 associated gene
No signs/symptoms info
Zonular cataract
Fatal infantile hypertonic myofibrillar myopathy

CRYAA
(UniProt - OMIM)
 CRYAB
(UniProt - OMIM)
CRYAB
(UniProt - OMIM)
CRYBA1
(UniProt - OMIM)
CRYBA4
(UniProt - OMIM)
CRYGB
(UniProt - OMIM)
CRYGC
(UniProt - OMIM)
CRYGD
(UniProt - OMIM)
HSF4
(UniProt - OMIM)
MIP
(UniProt - OMIM)

COMMON
GENES 		CRYAB
INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CRYAA
CRYBA1
CRYGC
CRYGD
MIP
(0.99)
(0.89)
(0.88)
(0.79)
(0.65)
CRYAB
CRYAB
CRYAB
CRYAB
CRYAB


Citations in the biomedical literature:


Zonular cataract
CRYAA CRYAB CRYBA1 CRYBA4 CRYGB CRYGC
CRYGD HSF4 MIP
Fatal infantile hypertonic myofibrillar myopathy



Zonular cataract
Fatal infantile hypertonic myofibrillar myopathy

Synonym(s):
- Lamellar cataract
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive
External references:
9 OMIM references -
1 MeSH reference: C535342
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.