Search Ontology:
Human Disease
retinitis pigmentosa 98
- Term ID
- DOID:0061109
- Synonyms
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- RP98
- Definition
- A retinitis pigmentosa characterized by onset of night blindness in early childhood, with gradual loss of peripheral vision and later of central vision that has_material_basis_in homozygous or compound heterozygous mutation in the TMEM216 gene on chromosome 11q12. https://pubmed.ncbi.nlm.nih.gov/39191256/
- References
- Ontology
- Human Disease ( DOID:0061109 )
- is a type of
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Genes Involved
Zebrafish Models