Warning: The NCBI web site requires JavaScript to function. more...

Full Report

Format

Full Report
Summary (Text)
Summary (XML)

Send to:

Choose Destination

File
Clipboard
Collections

Atypical Hemolytic Uremic Syndrome-4

MedGen UID:: 1788163
•Concept ID:: C5444421
•: Disease or Syndrome

Definition

An autosomal dominant subtype of atypical hemolytic uremic syndrome caused by mutation(s) in the CFB gene, encoding complement factor B. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVAtypical Hemolytic Uremic Syndrome-4

Abnormality of the genitourinary system
- Abnormality of the urinary system
  - Abnormality of the urinary system physiology
    - Abnormal renal physiology
      - Hemolytic-uremic syndrome
        Atypical hemolytic-uremic syndrome
        Atypical Hemolytic Uremic Syndrome-4

Supplemental Content

Table of contents

Recent activity

Clear Turn Off Turn On

Atypical Hemolytic Uremic Syndrome-4
Atypical Hemolytic Uremic Syndrome-4

MedGen

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...