Bombay Phenotype

Alias:
Bombay Phenotype, Digenic
[bombay Phenotype]
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Bombay Phenotype, also known as [bombay phenotype], is related to hemolytic disease due to fetomaternal alloimmunization and neutrophilia, hereditary. An important gene associated with Bombay Phenotype is FUT1 (Fucosyltransferase 1 (H Blood Group)), and among its related pathways/superpathways are Glycosaminoglycan metabolism and superpathway of glycosphingolipids biosynthesis. Affiliated tissues include placenta and neutrophil.

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
2
18
15

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

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CAS Number
Status
Phase
No data available

Disease Model

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

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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