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| Descriptor English: | Nephritis, Hereditary | ||||||
| Descriptor Spanish: |
Nefritis Hereditaria
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| 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 |
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| Tree number(s): |
C12.050.351.875.742 C12.050.351.968.419.570.620 C12.200.706.742 C12.200.777.419.570.620 C12.800.742 C12.950.419.570.620 C16.131.939.742 C17.300.200.517 |
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| 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. |
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| 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 |
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| Public MeSH Note: | 77; was ALPORT'S SYNDROME 1970-76 |
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| Online Note: | use NEPHRITIS, HEREDITARY to search ALPORT'S SYNDROME 1966-76 (as Prov 1966-69) |
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| History Note: | 77; was ALPORT'S SYNDROME 1964-76 (Prov 1964-69) |
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| 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 |
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Nephritis, Hereditary
- Preferred
Hemorrhagic Hereditary Nephritis
- Narrower
Alport Syndrome, Autosomal Recessive
- Narrower
Alport Syndrome, X-Linked
- Narrower
Alport Syndrome
- Narrower
Alport Syndrome, Autosomal Dominant
- Narrower
| 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 |
| 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 |
| Concept UI |
M0483244 |
| Preferred term | Alport Syndrome, Autosomal Recessive |
| Concept UI |
M0483242 |
| Preferred term | Alport Syndrome, X-Linked |
| Entry term(s) |
Alport Syndrome, X Linked X-Linked Alport Syndrome |
| 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 |
| Concept UI |
M0483243 |
| Preferred term | Alport Syndrome, Autosomal Dominant |
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