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Familial ocular anterior segment mesenchymal dysgenesis
1 OMIM reference -
2 associated genes
6 connected diseases
No signs/symptoms info
Disease Type of connection
Cataract-glaucoma
Congenital primary aphakia
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: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
FOXE3 Q13461601094
PITX3 O75364602669
No signs/symptoms info available.