Log In|Sign Up
ENRed Cell Phospholipid Defect with Hemolysis (HPCHA)
Alias:
High Red Cell Phosphatidylcholine Hemolytic Anemia
Phosphatidylcholine Red Cell Membrane Disorder
Leaky Red Cell Syndrome
Hpcha
Favorite
Red Cell Phospholipid Defect with Hemolysis, also known as high red cell phosphatidylcholine hemolytic anemia, is related to dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema and factor vii deficiency. Affiliated tissues include spleen, and related phenotypes are splenomegaly and reticulocytosis
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
