Non-neuropathic heredofamilial amyloidosis

Preferred Label : Non-neuropathic heredofamilial amyloidosis;

Inclusion CIM-10 : Hereditary amyloid nephropathy;

ICD-10 exclusion note : Transthyretin-related (ATTR) familial amyloid cardiomyopathy (E85.4);

Diag associé à un acte (%) : 72.8;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E850;

UMLS CUI

C0342611;

Automatic exact mappings (from CISMeF team)
- Familial Mediterranean Fever [NCIt concept]
- Hereditary amyloidosis with primary renal involvement [ORDO Disease]
- amyloidosis, familial visceral [MeSH Supplementary Concept]
- familial mediterranean fever [MeSH Descriptor]
- familial mediterranean fever [MeSH concept]
CISMeF manual mappings
- Familial non-neuropathic amyloidosis (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Non-neuropathic heredofamilial amyloidosis [ICD-11 Sub-sub category]
- Non-neuropathic heredofamilial amyloidosis [ICD-10 Sub-category (who)]
DO Cross reference
- CINCA Syndrome [DO Concept]
- autosomal dominant familial periodic fever [DO Concept]
Excluded by
- Hereditary nephropathy, not elsewhere classified [ICD-10 category]
- Peritonitis [ICD-10 category]
False automatic mappings
- CINCA Syndrome [DO Concept]
Manual NTBT mappings (CISMeF)
- AApoAI amyloidosis [ORDO Disease]
- AFib amyloidosis [ORDO Disease]
- ALys amyloidosis [ORDO Disease]
Metaterm(s)
- genetics [CISMeF Metaterm]
Orphanet concepts
- AApoAI amyloidosis [ORDO Disease]
- AApoAII amyloidosis [ORDO Disease]
- AFib amyloidosis [ORDO Disease]
- ALys amyloidosis [ORDO Disease]
- Amyloidosis [ORDO Disease]
- CINCA syndrome [ORDO Disease]
- Cryopyrin-associated periodic syndrome [ORDO Disease]
- Familial Mediterranean fever [ORDO Disease]
- Hereditary amyloidosis with primary renal involvement [ORDO Disease]
- Hereditary periodic fever syndrome [ORDO Disease]
- Hyperimmunoglobulinemia D with periodic fever [ORDO Disease]
- Infantile-onset periodic fever-panniculitis-dermatosis syndrome [ORDO Disease]
- Menstrual cycle-dependent periodic fever [ORDO Disease]
- Muckle-Wells syndrome [ORDO Disease]
- NLRP12-associated hereditary periodic fever syndrome [ORDO Disease]
- PFAPA syndrome [ORDO Disease]
- Periodic fever syndrome [ORDO Disease]
- Periodic fever syndrome of childhood [ORDO Disease]
- Periodic fever-infantile enterocolitis-autoinflammatory syndrome [ORDO Disease]
- Primary systemic amyloidosis [ORDO Disease]
- Tumor necrosis factor receptor 1 associated periodic syndrome [ORDO Disease]
- Unexplained periodic fever syndrome [ORDO Disease]
- Unexplained periodic fever syndrome of childhood [ORDO Disease]
See also inter- (CISMeF)
- Familial Mediterranean fever [ICD-11 Subcategory]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial non-neuropathic amyloidosis (disorder) [SNOMED CT concept]
- Non-neuropathic heredofamilial amyloidosis [ICD-11 Sub-sub category]

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