FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term retinitis pigmentosa 12 ID (Ontology) DOID:0110358 (Human Disease)
Definition A retinitis pigmentosa that has_material_basis_in mutation in the CRB1 gene on chromosome 1q31.3.
Also Known As "RP12"
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DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       1
Human Disease Models (FBhh)  DOID       1
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Relevant FlyBase reports
 Alleles Genes Human Disease Models
 retinitis pigmentosa 12       1      1      1
 for disease ribbon | retinitis pigmentosa 12       --       1       --
 model of | retinitis pigmentosa 12       1      1       --
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal recessive disease__
retinal degeneration             |
 |__retinitis pigmentosa_________|
                                 retinitis pigmentosa 12  3 rec.
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Is a autosomal recessive disease
retinitis pigmentosa
Part of
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Synonyms
  • "RP12" EXACT OMO:0003012
Secondary IDs
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ICD10CM:H35.5
MESH:C563999
MIM:600105