Bleeding Disorder, Platelet-Type, 17 (BDPLT17)

Alias:
Platelet-Type Bleeding Disorder 17
Bdplt17
Thrombasthenia-Thrombocytopenia, Hereditary
Hereditary Thrombasthenia-Thrombocytopenia
Autosomal Dominant Macrothrombocytopenia Gfi1b-Related
Autosomal Dominant Platelet Disorder Gfi1b-Related
Bleeding Disorder, Platelet Type 17
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Bleeding Disorder, Platelet-Type, 17, also known as platelet-type bleeding disorder 17, is related to myh-9 related disease and amegakaryocytic thrombocytopenia, congenital, 1. An important gene associated with Bleeding Disorder, Platelet-Type, 17 is GFI1B (Growth Factor Independent 1B Transcriptional Repressor). Affiliated tissues include bone marrow and bone, and related phenotypes are thrombocytopenia and epistaxis
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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7
54
5

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Mutations
No data available

Related Drugs

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Status
Phase
No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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