Skip to main content
Diseases

Hereditary nephritis

hereditary nephritis

Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Hereditary nephritis
Standard Disease Name
hereditary nephritis
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D009394
OMIM ID
MTHU031387
UMLS ID
C0027706
HPO ID
No data

Description and Extensions

Description
MSH2017_2016_08_12:A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
01
ACE
angiotensin I converting enzyme
angiotensin I converting enzyme
07
FCGRT
Fc fragment of IgG receptor and transporter
Fc fragment of IgG receptor and transporter