OMOP Concept 4128064
Thin basement membrane disease
StandardConditionSNOMED236418003Disorder
Maps from
5
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
5 source codes normalize to Thin basement membrane disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 124906 | Thin basement membrane disease | Non-standard |
| CIEL | 147893 | Benign familial hematuria | Non-standard |
| MeSH | C562476 | Hematuria, Benign Familial | Non-standard |
| Read | K024.00 | Thin basement membrane disease | Non-standard |
| Read | K197500 | Benign familial haematuria | Non-standard |
Synonyms
Alternative names recorded for Thin basement membrane disease across source vocabularies.
- Benign familial haematuria
- Benign familial hematuria
- enfermedad de membrana basal delgada
- enfermedad de membrana basal delgada (trastorno)
- hematuria familiar benigna
- nefropatía de membrana basal delgada
- Thin basement membrane disease (disorder)
- Thin basement membrane nephropathy
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(48)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Chronic glomerulonephritis
- 1Collagen IV nephropathy
- 1Kidney lesion
- 2Autosomal hereditary disorder
- 2Chronic disease of genitourinary system
- 2Chronic inflammatory disorder
- 2Glomerulonephritis
- 2Hereditary nephritis
- 2Kidney disease
- 2Secondary glomerular disease
- 2Urinary complication
- 3Chronic disease
- 3Disorder of kidney and/or ureter
- 3Disorder of retroperitoneum
- 3Disorder of the genitourinary system
- 3Disorder of urinary system
- 3Genetic disease of glomerulus
- 3Glomerular disease
- 3Hereditary disease
- 3Hereditary nephropathy
- 3Inflammatory disorder
- 3Kidney finding
- 3Nephritis
- 3Structural abnormality of renal corpuscle
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