Hemophagocytic Lymphohistiocytosis, Familial, 5, with or Without Microvillus Inclusion Disease (FHL5)

Alias:
Fhl5
Hemophagocytic Lymphohistiocytosis, Familial, 5, Without Microvillus Inclusion Disease
Lymphohistiocytosis, Hemophagocytic, Familial, Type 5
Familial Hemophagocytic Lymphohistiocytosis 5
Hplh5
Hlh5
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hemophagocytic Lymphohistiocytosis, Familial, 5, with or Without Microvillus Inclusion Disease, also known as fhl5, is related to migraine without aura and migraine with aura. An important gene associated with Hemophagocytic Lymphohistiocytosis, Familial, 5, with or Without Microvillus Inclusion Disease is STXBP2 (Syntaxin Binding Protein 2). Affiliated tissues include nk cells and liver.
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
5
31

Medical Symptom

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

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
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