Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due to (P5ND)

Alias:
Hemolytic Anemia Due to Pyrimidine 5' Nucleotidase Deficiency
P5n Deficiency
Anemia, Hemolytic, Due to Umph1 Deficiency
Hemolytic Anemia Due to Umph1 Deficiency
Hemolytic Anemia Due to P5n Deficiency
Umph1 Deficiency
Anemia, Hemolytic , Due to Uridine 5-Prime Monophosphate Hydrolase Deficiency
Pyrimidine 5-Prime Nucleotidase Deficiency, Hemolytic Anemia Due to
Uridine 5'-Monophosphate Hydrolase Deficiency
P5nd
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due to, also known as hemolytic anemia due to pyrimidine 5' nucleotidase deficiency, is related to porphyria, acute hepatic and hemolytic anemia. An important gene associated with Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due to is NT5C3A (5'-Nucleotidase, Cytosolic IIIA). Affiliated tissues include bone marrow and bone.

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
--
1
3
24

Medical Symptom

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

Gene & Mutation

#
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

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top