Disease #05120 (anemia (anemia))

Official abbreviation anemia
Name anemia
OMIM ID -
Inheritance -
Individuals reported having this disease 6
Phenotype entries for this disease 5
Associated with 1 gene NMNAT3
Associated tissues -
Disease features -
Remarks -
Date created 2016-01-23 01:57:01 +01:00 (CET)
Date last edited 2025-09-17 10:06:25 +02:00 (CEST)


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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     
00306851 P13 PubMed: Trabelsi 2021, Journal: Trabelsi 2021 - M no Tunisia - - - - - anemia, Gilbert syndrome Anemia, unconjugated hyperbilirubinemia, kernicterus UGT1A1 UGT1A1 1 1 Nawel Trabelsi
00326805 Fam3P18 PubMed: Trabelsi 2021, Journal: Trabelsi 2021 - M - Tunisia - - - - - anemia - PKLR, UGT1A1 PKLR, UGT1A1 7 1 Nawel Trabelsi
00430365 - - - M - China - - - - - anemia Splenomegaly,jaundice, anemia ANK1 ANK1 1 1 Chunli Wang
00430366 - - - F - China - - - - - anemia anemia ANK1 ANK1 1 1 Chunli Wang
00430367 - - - F - China - - - - - anemia anemia ANK1 ANK1 1 1 Chunli Wang
00466586 patient 2-generation family, 2 affected brothers, unaffected carrier mother Waanders, NVHG2025 T11 M - Netherlands - - - - - anemia mild hemolytic anemia - NMNAT3 1 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.