Cytoscape Web
Click node...

Granular corneal dystrophy type II
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Osteogenesis imperfecta type 4
6 OMIM references -
7 associated genes
No signs/symptoms info
Granular corneal dystrophy type II
Osteogenesis imperfecta type 4

TGFBI
(UniProt - OMIM)
 COL1A1
(UniProt - OMIM)
COL1A2
(UniProt - OMIM)
CRTAP
(UniProt - OMIM)
PPIB
(UniProt - OMIM)
SP7
(UniProt - OMIM)
TMEM38B
(UniProt - OMIM)
WNT1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TGFBI
TGFBI
(0.63)
(0.62)
COL1A1
COL1A2


Citations in the biomedical literature:


Granular corneal dystrophy type II
TGFBI
Osteogenesis imperfecta type 4
COL1A1 COL1A2 CRTAP PPIB SP7 TMEM38B
WNT1



Granular corneal dystrophy type II
Osteogenesis imperfecta type 4

Synonym(s):
- Avellino corneal dystrophy
- GCD2
- GCDII
- Granular corneal dystrophy type 2
- Granular-lattice corneal dystrophy
Synonym(s):
- OI type 4
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare odontologic disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: C535474
External references:
6 OMIM references -
1 MeSH reference: C536045
No signs/symptoms info available.