hereditary nephritis

Preferred Label : hereditary nephritis;

Détails

Origin ID

D7-12320;

UMLS CUI

C0027706;

Automatic exact mappings (from CISMeF team)
- Chronic hereditary nephritis [MedDRA LLT]
- Chronic hereditary nephritis [HPO term]
Currated CISMeF NLP mapping
- Alport syndrome [PASCAL descriptor]
- Alport syndrome [DO Concept]
- Alport syndrome [ICD-11 More detail]
- Alport's syndrome [MedDRA Preferred Term]
- Hereditary nephritis (disorder) [SNOMED CT concept]
- Other specified congenital malformation syndromes, not elsewhere classified [ICD-10 Sub-category]
- Other specified congenital malformation syndromes, not elsewhere classified [ICD-10 Sub-category (who)]
- alport syndrome [MeSH concept]
- hereditary nephritis [Radlex concept]
- hereditary nephritis [Disease (Nov.)]
- nephritis, hereditary [MeSH Descriptor]
- nephritis, hereditary [MeSH concept]
ICD-10 exact mapping(s)
- Hereditary nephropathy, not elsewhere classified | Unspecified [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Basement membrane disease [ORDO Disease]
- Lens shape anomaly [ORDO Disease]
- Renal disease with cataract [ORDO Disease]
- Syndromic genetic deafness [ORDO Disease]
Metaterm(s)
- nephrology [CISMeF Metaterm]
Référence SNOMED
- associated with [SNOMED Notion]
- deafness, nos [SNOMED Notion]
- disease, nos [SNOMED Notion]
- hematuria syndrome, nos [SNOMED Notion]
- kidney, nos [SNOMED Notion]
See also inter- (CISMeF)
- Alport syndrome [ORDO Disease]
- Zellweger syndrome [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Alport syndrome [DO Concept]
- Chronic hereditary nephritis [MedDRA LLT]
- Hereditary nephritis (disorder) [SNOMED CT concept]
- hereditary nephritis [Disease (Nov.)]
- nephritis, hereditary [MeSH Descriptor]
- nephritis, hereditary [MeSH concept]
Validated automatic mappings to BTNT
- Alport Syndrome [NCIt concept]
- Alport syndrome [Disease (Nov.)]

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