NM_000539.3(RHO):c.263T>C (p.Leu88Pro) AND Retinal dystrophy
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Oct 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003889887.1
Allele description [Variation Report for NM_000539.3(RHO):c.263T>C (p.Leu88Pro)]
NM_000539.3(RHO):c.263T>C (p.Leu88Pro)
Condition(s)
- Name:
- Retinal dystrophy
- Synonyms:
- Inherited retinal dystrophy
- Identifiers:
- MONDO: MONDO:0019118; MeSH: D058499; MedGen: C0854723; Human Phenotype Ontology: HP:0000556
Assertion and evidence details
Last Updated: Jun 23, 2024