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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

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

MedGen
Impaired urinary acidification
Impaired urinary acidification

MedGen
Combined cystic and ground-glass pattern on pulmonary HRCT
Combined cystic and ground-glass pattern on pulmonary HRCT

MedGen
Hearing loss, autosomal dominant 83
Hearing loss, autosomal dominant 83

MedGen
Impaired histidine renal tubular absorption
Impaired histidine renal tubular absorption

MedGen

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