Disease #01277 (OPA+ (atrophy, optic, plus syndrome (OPA+)), OMIM:125250)

Official abbreviation OPA+
Name atrophy, optic, plus syndrome (OPA+)
OMIM ID 125250
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 0
Associated with 1 gene OPA1
Associated tissues -
Disease features autosomal dominant
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00230995 - PubMed: Zerem 2019 - F no - - - 0 - - OPA, OPA+, OPA-1 Stroke (HP:0001297); Optic atrophy (HP:0000648); Progressive gait ataxia (HP:0007240); Dysarthria (HP:0001260); Tremor (HP:0001337); Specific learning disability (HP:0001328) - OPA1 2 1 Marc Ferre
Legend   How to query