Disease #01578 (THCYT1 (thrombocythemia, type 1), OMIM:187950)

Official abbreviation THCYT1
Name thrombocythemia, type 1
OMIM ID 187950
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 3 genes CALR, SH2B3, THPO
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-09-01 13:05:31 +02:00 (CEST)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00047224 - PubMed: Ernst 2010 - ? - - - - - - - THCYT1 Myelofibrosis (HP:0011974) EZH2 EZH2 1 1 Global Variome, with Curator vacancy
00047228 - PubMed: Ernst 2010 - M - - - - - - - THCYT1 Myelofibrosis (HP:0011974) EZH2 EZH2 1 1 Global Variome, with Curator vacancy
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