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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
B cell deficiency +  
B-cell neoplasm +  
basophil adenoma 
cancer-associated retinopathy 
cranial neuralgia +  
dendritic cell sarcoma +  
EBV-Positive T-Cell Lymphoproliferative Disorder of Childhood 
eosinophil disorder +  
eosinophil peroxidase deficiency 
functional neutrophil defect +  
hereditary neutrophilia 
human granulocytic anaplasmosis 
Lambert-Eaton myasthenic syndrome 
Langerhans Cell Histiocytosis 
leukostasis 
lymphopenia +  
Mastocytosis +  
neuralgic amyotrophy 
neutropenia +  
Opsoclonus-Myoclonus Syndrome 
paraneoplastic cerebellar degeneration 
paraneoplastic polyneuropathy 
phagocyte bactericidal dysfunction +  
POEMS syndrome 
A multisystemic disorder characterized by a sensorimotor polyneuropathy (POLYNEUROPATHIES), organomegaly, endocrinopathy, monoclonal gammopathy, and pigmentary skin changes. Other clinical features which may be present include EDEMA; CACHEXIA; microangiopathic glomerulopathy; pulmonary hypertension (HYPERTENSION, PULMONARY); cutaneous necrosis; THROMBOCYTOSIS; and POLYCYTHEMIA. This disorder is frequently associated with osteosclerotic myeloma. (From Adams et al., Principles of Neurology, 6th ed, p1335; Rev Med Interne 1997;18(7):553-62) POEMS syndrome is a paraneoplastic syndrome characterized by polyradiculoneuropathy (P), organomegaly (O), endocrinopathy (E), clonal plasma cell disorder (M), and skin changes (S). Other features include papilledema, extravascular volume overload, sclerotic bone lesions, thrombocytosis/erythrocytosis, and elevated VEGF levels.
radiation-induced plexopathy 
Small Intestinal Enteropathy-Associated T-Cell Lymphoma 
Subcutaneous Panniculitis-Like T-Cell Lymphoma 
T-cell leukemia +  
thymoma type B +  

Synonyms
Exact Synonyms: Crow-Fukase syndrome ;   PEP syndrome ;   POEMS syndrome (disorder) ;   Takatsuki syndrome ;   osteosclerotic myeloma ;   polyneuropathy-endocrinopathy-plasma cell dyscrasia syndrome
Related Synonyms: polyneuropathy organomegaly ;   polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes syndrome
Xrefs: DOID:14039 ;   GARD:7411 ;   MESH:D016878 ;   MONDO:0017364 ;   MedDRA:10053869 ;   NANDO:1200033 ;   NCI:C80303 ;   NORD:1586 ;   ORDO:2905 ;   SCTID:79268002 ;   SNOMEDCT:79268002 ;   UMLS:C0085404
External Ontologys: disease_has_location EFO:CL:0000786
Definition Sources: Orphanet:2905, PMID:23398538

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