loading...| 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 |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000002367 |
|
| 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 |
|
| cui |
C0031069 |
|
| May be treated by |
http://purl.bioontology.org/ontology/NDFRT/N0000148926 http://purl.bioontology.org/ontology/NDFRT/N0000191111 |
|
| 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. |
|
| MESH DUI |
D010505 |
|
| MeSH name |
Familial Mediterranean Fever |
|
| MESH UI |
M0016320 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000002367 |
|
| NUI |
N0000002367 |
|
| prefLabel |
Familial Mediterranean Fever [Disease/Finding] |
|
| SNOMED CID |
12579009 |
|
| tui |
T047 |
|
| subClassOf |