Search Ontology:
Human Disease

cataract 36

Term ID
DOID:0110247
Synonyms
  • autosomal recessive congenital cataract 4
  • CATC4
  • CTRCT36
Definition
A cataract that has_material_basis_in homozygous mutation in the TDRD7 gene on chromosome 9q22.33. https://www.ncbi.nlm.nih.gov/pubmed/21436445
References
Ontology
Human Disease   ( DOID:0110247 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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