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Descriptor English: Nephritis, Hereditary
Descriptor Spanish: Nefritis Hereditaria
Descriptor Portuguese: Nefrite Hereditária
Descriptor French: Néphropathie familiale avec surdité
Entry term(s): Alport Syndrome
Alport Syndrome, Autosomal Dominant
Alport Syndrome, Autosomal Recessive
Alport Syndrome, X Linked
Alport Syndrome, X-Linked
Alport's Syndrome
Congenital Hereditary Hematuria
Familial Nephritis
Hematuria Nephropathy Deafness Syndrome
Hematuria, Congenital Hereditary
Hematuria-Nephropathy-Deafness Syndrome
Hematuric Hereditary Nephritis
Hemorrhagic Familial Nephritis
Hemorrhagic Hereditary Nephritis
Hereditary Familial Congenital Hemorrhagic Nephritis
Hereditary Hematuria Syndrome
Hereditary Interstitial Pyelonephritis
Hereditary Nephritis
Nephritis, Familial
Nephritis, Hematuric Hereditary
Nephritis, Hemorrhagic Familial
Nephritis, Hemorrhagic Hereditary
Pyelonephritis, Hereditary Interstitial
Syndrome, Alport
Syndrome, Hematuria-Nephropathy-Deafness
X-Linked Alport Syndrome
Tree number(s): C12.706.742
C12.777.419.570.620
C13.351.875.742
C13.351.968.419.570.620
C16.131.939.742
C17.300.200.517
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D009394
Scope note: 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.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Public MeSH Note: 77; was ALPORT'S SYNDROME 1970-76
Online Note: use NEPHRITIS, HEREDITARY to search ALPORT'S SYNDROME 1966-76 (as Prov 1966-69)
History Note: 77; was ALPORT'S SYNDROME 1964-76 (Prov 1964-69)
DeCS ID: 9587
Unique ID: D009394
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1970/01/01
Date of Entry: 1999/01/01
Revision Date: 2013/07/08
Nephritis, Hereditary - Preferred
Concept UI M0014627
Scope note 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.
Preferred term Nephritis, Hereditary
Entry term(s) Familial Nephritis
Hereditary Interstitial Pyelonephritis
Hereditary Nephritis
Nephritis, Familial
Pyelonephritis, Hereditary Interstitial
Hemorrhagic Hereditary Nephritis - Narrower
Concept UI M0532945
Preferred term Hemorrhagic Hereditary Nephritis
Entry term(s) Congenital Hereditary Hematuria
Hematuria, Congenital Hereditary
Hematuric Hereditary Nephritis
Hemorrhagic Familial Nephritis
Hereditary Familial Congenital Hemorrhagic Nephritis
Hereditary Hematuria Syndrome
Nephritis, Hematuric Hereditary
Nephritis, Hemorrhagic Familial
Nephritis, Hemorrhagic Hereditary
Alport Syndrome, Autosomal Recessive - Narrower
Concept UI M0483244
Preferred term Alport Syndrome, Autosomal Recessive
Alport Syndrome, X-Linked - Narrower
Concept UI M0483242
Preferred term Alport Syndrome, X-Linked
Entry term(s) Alport Syndrome, X Linked
X-Linked Alport Syndrome
Alport Syndrome - Narrower
Concept UI M0483241
Preferred term Alport Syndrome
Entry term(s) Alport's Syndrome
Hematuria Nephropathy Deafness Syndrome
Hematuria-Nephropathy-Deafness Syndrome
Syndrome, Alport
Syndrome, Hematuria-Nephropathy-Deafness
Alport Syndrome, Autosomal Dominant - Narrower
Concept UI M0483243
Preferred term Alport Syndrome, Autosomal Dominant



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