Disease #05363 (ANOA;MMDS9A (neuropathy, auditory, and optic atrophy), OMIM:617717)

Official abbreviation ANOA;MMDS9A
Name neuropathy, auditory, and optic atrophy
OMIM ID 617717
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene FDXR
Associated tissues -
Disease features autosomal recessive
Remarks -
Date created 2017-12-29 14:15:12 +01:00 (CET)
Date last edited 2024-11-25 10:17:09 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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     
00147019 Fam1 PubMed: Paul 2017 3-generation family, 4 affecteds (4F), unaffected heterozygous carrier parents/relatives F yes Tunisia - - - - - ANOA;MMDS9A see paper; ... FDXR FDXR 1 4 Johan den Dunnen
00147020 Fam2Pat5 PubMed: Paul 2017 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M no Algeria - - - - - ANOA;MMDS9A see paper; ... FDXR FDXR 2 1 Johan den Dunnen
00147021 Fam3Pat6 PubMed: Paul 2017 2-generation family, 1 affected, unaffected heterozygous carrier parents M no France - - - - - ANOA;MMDS9A see paper; ... FDXR FDXR 2 1 Johan den Dunnen
00147022 Fam3Pat7/8 PubMed: Paul 2017 2-generation family, 2 affecteds (2F), unaffected heterozygous carrier parents F no Azerbaijan;Russia - - - - - ANOA;MMDS9A see paper; ... FDXR FDXR 2 2 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.