CD38, CD38 molecule, 952

N. diseases: 473; N. variants: 7
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: C1282310
Disease: Intermittent pain
Intermittent pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 1 0.010 None 1.000 1 2017 2017
CUI: C1334377
Disease: Laryngeal Sarcoma
Laryngeal Sarcoma
disease Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Neoplastic Process 1 0.010 None 1.000 1 2004 2004
Acute Hemolytic Transfusion Reaction
disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 1 3 0.010 None 1.000 1 1990 1990
Prolapsed thoracic intervertebral disc
phenotype Respiratory Tract Diseases Acquired Abnormality 2 0.020 None 1.000 2 2018 2019
CUI: C0232492
Disease: Upper abdominal pain
Upper abdominal pain
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Sign or Symptom 2 0.010 None 1.000 1 2018 2018
CUI: C0520962
Disease: Localized pain
Localized pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 2 0.010 None 1.000 1 2017 2017
CUI: C0795805
Disease: Chromosome 2, trisomy 2q
Chromosome 2, trisomy 2q
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 2 0.010 None 1.000 1 1977 1977
CUI: C2585107
Disease: Asymptomatic multiple myeloma
Asymptomatic multiple myeloma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process 2 0.010 None 1.000 1 2018 2018
CUI: C2700593
Disease: Cystic dermoid choristoma
Cystic dermoid choristoma
phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 2 0.010 None 1.000 1 2019 2019
CUI: C3900051
Disease: Amotivation
Amotivation
phenotype Sign or Symptom 2 0.010 None 1.000 1 2018 2018
CUI: C0264192
Disease: Pelvic obliquity
Pelvic obliquity
phenotype Musculoskeletal Diseases Acquired Abnormality 3 0.010 None 1.000 1 2017 2017
CUI: C1960447
Disease: Hypergonadotropic amenorrhea
Hypergonadotropic amenorrhea
disease Disease or Syndrome 3 0.010 None 1.000 1 2009 2009
CUI: C0038604
Disease: Subungual exostoses
Subungual exostoses
disease Neoplasms; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Neoplastic Process 4 0.030 None 1.000 3 2004 2011
CUI: C1334801
Disease: Monophasic Synovial Sarcoma
Monophasic Synovial Sarcoma
disease Neoplasms Neoplastic Process 4 0.020 None 1.000 2 1996 2002
CUI: C0015458
Disease: Facial Hemiatrophy
Facial Hemiatrophy
disease Nervous System Diseases; Stomatognathic Diseases Disease or Syndrome 4 4 0.010 None 1.000 1 2 2010 2010
CUI: C2363750
Disease: MDS transformation
MDS transformation
disease Neoplastic Process 4 0.010 None 1.000 1 2002 2002
CUI: C0036310
Disease: Scheuermann's Disease
Scheuermann's Disease
disease Musculoskeletal Diseases Disease or Syndrome 5 1 0.010 None 1.000 1 2019 2019
CUI: C0231616
Disease: Beevor's sign
Beevor's sign
phenotype Sign or Symptom 5 0.010 None 1.000 1 2018 2018
CUI: C0266798
Disease: Compression of umbilical cord
Compression of umbilical cord
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 5 0.010 None 1.000 1 2002 2002
CUI: C0795809
Disease: Chromosome 3, trisomy 3q
Chromosome 3, trisomy 3q
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 5 0.010 None 1.000 1 1981 1981
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 8 15 0.010 None 1.000 1 1996 1996
Hyperostosis, Diffuse Idiopathic Skeletal
disease Musculoskeletal Diseases Disease or Syndrome 9 0.010 None 1.000 1 2018 2018
CUI: C2748518
Disease: Lumbar scoliosis
Lumbar scoliosis
disease Disease or Syndrome 10 2 0.010 None 1.000 1 2018 2018
CUI: C0268301
Disease: Reifenstein Syndrome
Reifenstein Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 11 35 0.010 None 1.000 1 2004 2004