Multiple myeloma

Symptom Information:

Symptom ID: HPO:0006775
Synonyms:
Plasmocytoma [HPO:0006775]
Multiple myeloma (disorder) [Orphanet:51050]
Multiple myeloma, no ICD-O subtype (morphologic abnormality) [Orphanet:51050]
Multiple Myeloma [Orphanet:51050]
Multiple myeloma [OMIM:Multiple myeloma]
Multiple myeloma [Orphanet:51050]
Plasma cell myeloma [MedDRA:10035226]
IGA myeloma [MedDRA:10035226]
IGD myeloma [MedDRA:10035226]
IGE myeloma [MedDRA:10035226]
IGG myeloma [MedDRA:10035226]
Multiple myeloma [MedDRA:10035226]
Multiple myeloma and immunoproliferative neoplasms [MedDRA:10035226]
Multiple myeloma myelomatosis [MedDRA:10035226]
Multiple myeloma without mention of remission [MedDRA:10035226]
Myeloma [MedDRA:10035226]
Myeloma, malignant [MedDRA:10035226]
Myelomatosis [MedDRA:10035226]
Myelomatosis multiple [MedDRA:10035226]
Nonsecretory myeloma [MedDRA:10035226]
Multiple myeloma progression [MedDRA:10035226]
Multiple myeloma transformation [MedDRA:10035226]
Multiple myelomas [MedDRA:10028229]
Quality:
Cross references:
Orphanet:51050 "Multiple myeloma" [Orphanet:51050]
OMIM: "Multiple myeloma" [OMIM:Multiple myeloma]
UMLS:C0026764 "Multiple Myeloma" [Orphanet:51050]
Is a (Direct Parents):
MedDRA Plasma cell neoplasms
Orphanet Lymphoma
HPO         Hematological neoplasm
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Hematological neoplasm(HPO:0004377)
                Multiple myeloma(HPO:0006775)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Hematological neoplasm(HPO:0004377)
             Multiple myeloma(HPO:0006775)
MedDRA:
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Plasma cell neoplasms(MedDRA:10035227)
       Multiple myeloma(HPO:0006775)
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

AL amyloidosis (Orphanet:85443)
Acquired ichthyosis (Orphanet:454)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Lichen amyloidosis (Orphanet:49804)
Multiple myeloma (Orphanet:29073)
Primary systemic amyloidosis (Orphanet:314701)
Subcorneal pustular dermatosis (Orphanet:48377)
Systemic capillary leak syndrome (Orphanet:188)