Search Ontology:
Human Disease

cataract 35

Term ID
DOID:0110261
Synonyms
  • autosomal recessive congenital nuclear cataract 1
  • cataract 35, congenital nuclear
  • CATCN1
  • CTRCT35
Definition
A cataract that has_material_basis_in variation in the region 19q13. https://www.ncbi.nlm.nih.gov/pubmed/15671291
References
Ontology
Human Disease   ( DOID:0110261 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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