CD6, CD6 molecule, 923

N. diseases: 216; N. variants: 8
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: C0085222
Disease: Psoas Abscess
Psoas Abscess
disease Infections Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C0270679
Disease: Brain stem herniation
Brain stem herniation
phenotype Anatomical Abnormality 1 0.010 None 1.000 1 2017 2017
CUI: C0270771
Disease: Syringobulbia
Syringobulbia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 1 0.010 None 1.000 1 2018 2018
Childhood L2 Acute Lymphoblastic Leukemia
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 1 0.010 None 1.000 1 2003 2003
CUI: C1367539
Disease: Giant cell angiofibroma
Giant cell angiofibroma
disease Neoplasms Neoplastic Process 1 0.010 None 1.000 1 2006 2006
CUI: C0581321
Disease: Vertebral osteoporosis
Vertebral osteoporosis
disease Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
Cellular Congenital Mesoblastic Nephroma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 2 0.010 None < 0.001 1 2001 2001
tumor miofibroblástico peribronquial congénito
disease Neoplastic Process 3 0.010 None 1.000 1 2008 2008
Clear cell sarcoma, of tendons and aponeuroses
disease Neoplasms Neoplastic Process 4 0.020 None 1.000 2 1993 1996
CUI: C0279737
Disease: low-grade salivary gland carcinoma
low-grade salivary gland carcinoma
disease Neoplastic Process 4 0.010 None 1.000 1 2017 2017
CUI: C1861923
Disease: Acampomelic Campomelic Dysplasia
Acampomelic Campomelic Dysplasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 4 3 0.010 None 1.000 1 1996 1996
CUI: C0266798
Disease: Compression of umbilical cord
Compression of umbilical cord
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 5 0.020 None 1.000 2 1984 2017
CUI: C0007659
Disease: Cementoma
Cementoma
disease Neoplasms Neoplastic Process 5 1 0.010 None 1.000 1 1996 1996
CUI: C0231616
Disease: Beevor's sign
Beevor's sign
phenotype Sign or Symptom 5 0.010 None 1.000 1 2018 2018
CUI: C0795816
Disease: Chromosome 6, monosomy 6q
Chromosome 6, monosomy 6q
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 5 0.010 None 1.000 1 1998 1998
CUI: C0346200
Disease: Intravenous leiomyomatosis
Intravenous leiomyomatosis
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 6 0.010 None 1.000 1 2002 2002
Bilateral Periventricular Nodular Heterotopia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 6 1 0.010 None 1.000 1 2008 2008
CUI: C4707057
Disease: Tetrasomy 21
Tetrasomy 21
disease Disease or Syndrome 6 0.010 None 1.000 1 2000 2000
CUI: C0334551
Disease: Myxoid chondrosarcoma
Myxoid chondrosarcoma
disease Neoplasms Neoplastic Process 9 0.010 None 1.000 1 1996 1996
CUI: C1306242
Disease: Aggressive angiomyxoma
Aggressive angiomyxoma
disease Neoplasms Neoplastic Process 9 0.010 None 1.000 1 2008 2008
Adult Clear Cell Sarcoma of Soft Parts
disease Neoplasms Neoplastic Process 10 0.020 None 1.000 2 2004 2006
Childhood Clear Cell Sarcoma of Soft Parts
disease Neoplasms Neoplastic Process 10 0.020 None 1.000 2 2004 2006
CUI: C4041089
Disease: Poorly differentiated sarcoma
Poorly differentiated sarcoma
disease Neoplasms Neoplastic Process 11 0.010 None 1.000 1 1992 1992
CUI: C0028643
Disease: Numbness
Numbness
phenotype Nervous System Diseases; Mental Disorders Sign or Symptom 12 2 0.020 None 1.000 2 2017 2020
CUI: C1855418
Disease: Thoracolumbar kyphosis
Thoracolumbar kyphosis
disease Anatomical Abnormality 13 0.010 None 1.000 1 2018 2018