Disease #04625 (HSAN8 (neuropathy, sensory and autonomic, hereditary, type VIII (HSAN-8)), OMIM:616488)

Official abbreviation HSAN8
Name neuropathy, sensory and autonomic, hereditary, type VIII (HSAN-8)
OMIM ID 616488
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PRDM12
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


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     
00081097 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - HSAN8 Neuropathy, hereditary sensory and autonomic, type VIII (OMIM:616488) PRDM12 PRDM12 1 1 Daniel Trujillano
Legend   How to query  


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