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Cataract-glaucoma
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Familial ocular anterior segment mesenchymal dysgenesis
Posterior polar cataract
Translocation renal cell carcinoma
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
Young adult-onset Parkinsonism
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
PITX3 O75364602669
No signs/symptoms info available.