WAS, WASP actin nucleation promoting factor, 7454

N. diseases: 204; N. variants: 37
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: C0018926
Disease: Hematemesis
Hematemesis
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Sign or Symptom 14 1 0.100 None 0
CUI: C0025222
Disease: Melena
Melena
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Pathologic Function 15 1 0.100 None 0 1
Insulin-dependent diabetes mellitus secretory diarrhea syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 16 18 0.010 None < 0.001 1 2000 2000
CUI: C0278080
Disease: Physical addiction
Physical addiction
disease Chemically-Induced Disorders; Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 18 0.010 None 1.000 1 2019 2019
CUI: C0851886
Disease: Pneumocystis Infections
Pneumocystis Infections
group Infections Disease or Syndrome 18 0.010 None 1.000 1 2004 2004
CUI: C0272278
Disease: Congenital thrombocytopenia
Congenital thrombocytopenia
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 19 3 0.130 None 1.000 3 1995 2015
CUI: C0855740
Disease: Abnormal platelet function
Abnormal platelet function
phenotype Finding 21 2 0.100 None 0
CUI: C4025218
Disease: Vasculitis of large artery
Vasculitis of large artery
disease Cardiovascular Diseases Disease or Syndrome 21 0.100 None 0
Recurrent lower respiratory tract infection
phenotype Disease or Syndrome 23 0.100 None 0
CUI: C4021745
Disease: Abnormality of the musculature
Abnormality of the musculature
phenotype Anatomical Abnormality 24 0.100 None 0
CUI: C1839163
Disease: THROMBOCYTOPENIA 1 (disorder)
THROMBOCYTOPENIA 1 (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 30 18 0.800 strong 1.000 68 16 1995 2019
CUI: C1279296
Disease: Chronic leukemia (category)
Chronic leukemia (category)
disease Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 32 0.100 None 0
CUI: C4316909
Disease: Marijuana Use
Marijuana Use
disease Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 33 0.010 None 1.000 1 2018 2018
CUI: C1697453
Disease: Spontaneous hematomas
Spontaneous hematomas
disease Disease or Syndrome 33 0.100 None 0
CUI: C0685891
Disease: Congenital hypoplasia of thymus
Congenital hypoplasia of thymus
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 34 0.100 None 0
CUI: C0018932
Disease: Hematochezia
Hematochezia
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 37 12 0.100 None 0
X-Linked Combined Immunodeficiency Diseases
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 38 42 0.010 None 1.000 1 2002 2002
CUI: C0037354
Disease: Smallpox
Smallpox
disease Infections Disease or Syndrome 39 0.010 None 1.000 1 2005 2005
CUI: C0151529
Disease: Prolonged bleeding time
Prolonged bleeding time
phenotype Finding 39 3 0.100 None 0
CUI: C0006870
Disease: Cannabis Dependence
Cannabis Dependence
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 40 13 0.010 None 1.000 1 2019 2019
CUI: C0151699
Disease: Intracranial Hemorrhage
Intracranial Hemorrhage
group Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 40 2 0.100 None 0
CUI: C0007370
Disease: Catalepsy
Catalepsy
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Mental or Behavioral Dysfunction 43 0.030 None 1.000 3 2015 2020
CUI: C0017565
Disease: Gingival Hemorrhage
Gingival Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms; Stomatognathic Diseases Pathologic Function 50 2 0.100 None 0
CUI: C0020492
Disease: Hyperostosis
Hyperostosis
disease Musculoskeletal Diseases Disease or Syndrome 50 3 0.100 None 0
Iron-Refractory Iron Deficiency Anemia
disease Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 51 36 0.100 None 0