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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
| Id | http://purl.bioontology.org/ontology/NDFRT/N0000002367
http://purl.bioontology.org/ontology/NDFRT/N0000002367
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|---|---|
| Preferred Name | Familial Mediterranean Fever [Disease/Finding] |
| Synonyms |
Familial Paroxysmal Polyserositis
Wolff's Periodic Disease
Familial Mediterranean Fever
Wolff Periodic Disease
Benign Paroxysmal Peritonitis
Periodic Disease
Periodic Disease, Wolff's
Polyserositis, Familial Paroxysmal
Recurrent Polyserositis
Polyserositis, Recurrent
Periodic Peritonitis
Mediterranean Fever, Familial
Familial Mediterranean Fever, Autosomal Recessive
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
Familial Paroxysmal Polyserositis
Wolff's Periodic Disease
Familial Mediterranean Fever
Wolff Periodic Disease
Benign Paroxysmal Peritonitis
Periodic Disease
Periodic Disease, Wolff's
Polyserositis, Familial Paroxysmal
Recurrent Polyserositis
Polyserositis, Recurrent
Periodic Peritonitis
Mediterranean Fever, Familial
Familial Mediterranean Fever, Autosomal Recessive
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See less
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|---|---|
| prefLabel | Familial Mediterranean Fever [Disease/Finding]
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| notation | N0000002367
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| May be treated by | |
| MESH DEFINITION | A group of HEREDITARY AUTOINFLAMMATION DISEASES, characterized by recurrent fever, abdominal pain, headache, rash, PLEURISY; and ARTHRITIS. ORCHITIS; benign MENINGITIS; and AMYLOIDOSIS may also occur. Homozygous or compound heterozygous mutations in marenostrin gene result in autosomal recessive transmission; simple heterozygous, autosomal dominant form of the disease.
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| MESH UI | M0016320
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| subClassOf | |
| Semantic type UMLS property | |
| MeSH name | Familial Mediterranean Fever
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| NDFRT kind | DISEASE_KIND
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| type | |
| SNOMED CID | 12579009
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| tui | T047
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| NUI | N0000002367
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| cui | C0031069
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| MESH DUI | D010505
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| Delete | Subject | Author | Type | Created |
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| No notes to display |