CCND1, cyclin D1, 595

N. diseases: 859; N. variants: 12
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0015967
Disease: Fever
Fever
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 1021 66 0.100 None 0
Papillary cystadenoma of the epididymis
disease Neoplastic Process 6 0.100 None 0
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
phenotype Pathological Conditions, Signs and Symptoms Finding 345 19 0.100 None 0
Abnormality of the gastrointestinal tract
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Anatomical Abnormality 14 1 0.100 None 0
CUI: C0544886
Disease: Somatic mutation
Somatic mutation
phenotype Cell or Molecular Dysfunction 151 0.100 None 0
Functional abnormality of the gastrointestinal tract
phenotype Pathologic Function 7 0.100 None 0
COLORECTAL CANCER, SUSCEPTIBILITY TO
phenotype Finding 3 8 0.100 None 0 1
CUI: C0032461
Disease: Polycythemia
Polycythemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 82 22 0.100 None 0
CUI: C0032227
Disease: Pleural effusion disorder
Pleural effusion disorder
group Respiratory Tract Diseases Disease or Syndrome 227 14 0.100 None 0
CUI: C0040264
Disease: Tinnitus
Tinnitus
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 103 14 0.100 None 0
CUI: C4552811
Disease: Generalized Muscle Weakness, CTCAE
Generalized Muscle Weakness, CTCAE
phenotype Finding 117 0.100 None 0
CUI: C0037926
Disease: Compression of spinal cord
Compression of spinal cord
disease Nervous System Diseases; Wounds and Injuries Disease or Syndrome 60 2 0.100 None 0
CUI: C0037859
Disease: Spermatocele
Spermatocele
disease Pathological Conditions, Signs and Symptoms; Male Urogenital Diseases Disease or Syndrome 5 0.100 None 0
CUI: C0431718
Disease: Multiple renal cysts
Multiple renal cysts
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 46 4 0.100 None 0
CUI: C4048270
Disease: Decreased antibody level in blood
Decreased antibody level in blood
phenotype Finding 75 5 0.100 None 0
Compression fracture of vertebral column
phenotype Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Wounds and Injuries Pathologic Function 25 1 0.100 None 0
MULTIPLE MYELOMA, t(11;14) TYPE, SUSCEPTIBILITY TO
phenotype Finding 1 1 0.100 None 0 1
Sensorineural Hearing Loss (disorder)
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 783 111 0.100 None 0
VON HIPPEL-LINDAU SYNDROME, MODIFIER OF
phenotype Finding 1 1 0.100 None 0 1
CUI: C4024223
Disease: Spinal hemangioblastoma
Spinal hemangioblastoma
disease Neoplasms; Nervous System Diseases Neoplastic Process 2 1 0.100 None 0
CUI: C0241240
Disease: Tall stature
Tall stature
phenotype Finding 79 14 0.100 None 0
CUI: C2609414
Disease: Acute kidney injury
Acute kidney injury
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Injury or Poisoning 185 3 0.100 None 0
CUI: C0020437
Disease: Hypercalcemia
Hypercalcemia
disease Nutritional and Metabolic Diseases Disease or Syndrome 157 9 0.100 None 0
CUI: C0016663
Disease: Pathological fracture
Pathological fracture
phenotype Wounds and Injuries Pathologic Function 35 2 0.100 None 0
CUI: C0030554
Disease: Paresthesia
Paresthesia
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 121 8 0.100 None 0