Disease #07212 (FMAIT2 (fetomaternal alloimmune thrombocytopenia, type 2), OMIM:621266)

Official abbreviation FMAIT2
Name fetomaternal alloimmune thrombocytopenia, type 2
OMIM ID 621266
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease 2
Associated with 1 gene ITGA2B
Associated tissues -
Disease features -
Remarks -
Date created 2025-12-08 19:41:19 +01:00 (CET)
Date last edited 2025-12-13 19:00:12 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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     
00470924 patient PubMed: Noris 1995 2-generation family, 1 affected, unaffected heterozygous carrier father F - Italy - - - - - FMAIT2 see paper; ..., birth-petechiae, extensive hematomas, no hepatomegaly, no splenomegaly, no nfections, no neurologic damage, platelet count 6×10+9/L ITGA2B ITGA2B 1 1 Johan den Dunnen
00470925 patient PubMed: Poles 2013 2-generation family, 1 affected, unaffected heterozygous carrier father - - Ireland - - - - - FMAIT2 see paper; ..., severe thrombocytopenia, platelet count 17×10+9/L, petechiae ITGA2B ITGA2B 1 1 Johan den Dunnen
00470926 patient - - - - - - - - - - FMAIT2 - ITGA2B ITGA2B 1 1 Johan den Dunnen
00470927 patient - - - - - - - - - - FMAIT2 - ITGA2B ITGA2B 1 1 Johan den Dunnen
00470928 patient - - - - - - - - - - FMAIT2 - ITGA2B ITGA2B 1 1 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.