Disease #02112 (TYRSN1 (tyrosinemia, type I), OMIM:276700)

Official abbreviation TYRSN1
Name tyrosinemia, type I
OMIM ID 276700
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene FAH
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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     
00073740 - - - F yes Kuwait Middle Eastern - - - - TYRSN1 - FAH FAH 1 1 Patrick R. Blackburn
00419319 patient - - - - China - - - - - TYRSN1 - FAH FAH 1 1 Jiao Chen
Legend   How to query  


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