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Multiple myeloma
1 OMIM reference -
1 associated gene
62 connected diseases
No signs/symptoms info
Disease Type of connection
B-cell chronic lymphocytic leukemia
Mantle cell lymphoma
Multiple endocrine neoplasia type 1
Familial melanoma
Familial pancreatic carcinoma
Peripheral resistance to thyroid hormones
Precursor B-cell acute lymphoblastic leukemia
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Autosomal recessive primary microcephaly
Multiple endocrine neoplasia type 4
Complete androgen insensitivity syndrome
Estrogen resistance syndrome
Familial hypospadias
Familial retinoblastoma
Kennedy disease
Monosomy 13q14
Partial androgen insensitivity syndrome
Unilateral retinoblastoma
X-linked dystonia-parkinsonism
Familial prostate cancer
Hereditary breast and ovarian cancer syndrome
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Primary peritoneal carcinoma
Autosomal dominant hyper-IgE syndrome
Melanoma and neural system tumor syndrome
Melanoma-pancreatic cancer syndrome
Precursor T-cell acute lymphoblastic leukemia
Generalized resistance to thyroid hormone
Selective pituitary resistance to thyroid hormone
Beckwith-Wiedemann syndrome due to CDKN1C mutation
IMAGe syndrome
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
Lymphangioleiomyomatosis
Tuberous sclerosis
MODY syndrome
Alpha-crystallinopathy
Ear-patella-short stature syndrome
Familial isolated dilated cardiomyopathy
Fatal infantile hypertonic myofibrillar myopathy
Posterior polar cataract
Zonular cataract
Split hand-split foot malformation
3M syndrome
Distal 22q11.2 microdeletion syndrome
Familial lipoprotein lipase deficiency
Hyperlipoproteinemia type 5
Persistent polyclonal B-cell lymphocytosis
Severe combined immunodeficiency due to CARD11 deficiency
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Catecholaminergic polymorphic ventricular tachycardia
Chronic myeloid leukemia
Familial platelet syndrome with predisposition to acute myelogenous leukemia
Isolated delta-storage pool disease
Pseudohypoaldosteronism type 2E
Synonym(s):
- Kahler's disease
- Medullary plasmacytoma
- Myelomatosis
- Plasma cell myeloma
Classification (Orphanet):
- Rare hematologic disease
- Rare neurologic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: D009101
Gene symbol UniProt reference OMIM reference
CCND1 P24385168461
No signs/symptoms info available.