IFNGR1, interferon gamma receptor 1, 3459

N. diseases: 153; N. variants: 30
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: C0011991
Disease: Diarrhea
Diarrhea 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 632 63 0.100 None 0
CUI: C3266863
Disease: Atypical Mycobacteriosis, Familial
Atypical Mycobacteriosis, Familial 		disease Infections Disease or Syndrome 1 0.300 None 0
CUI: C1112429
Disease: Interferon gamma receptor deficiency
Interferon gamma receptor deficiency 		disease Disease or Syndrome 2 1 0.100 None 0 1
CUI: C0152491
Disease: Salmonella osteomyelitis
Salmonella osteomyelitis 		disease Infections; Musculoskeletal Diseases Disease or Syndrome 1 0.100 None 0
CUI: C0151632
Disease: ESR raised
ESR raised 		phenotype Finding 36 0.100 None 0
CUI: C1608955
Disease: Mycobacterium abscessus Infection
Mycobacterium abscessus Infection 		disease Infections Disease or Syndrome 6 0.300 None 0
CUI: C0015967
Disease: Fever
Fever 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 1021 66 0.100 None 0
CUI: C0151379
Disease: Rheumatoid factor positive (finding)
Rheumatoid factor positive (finding) 		phenotype Laboratory or Test Result 7 0.100 None 0
CUI: C0032285
Disease: Pneumonia
Pneumonia 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 1032 33 0.100 None 0
CUI: C1834752
Disease: MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)
MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding) 		disease Finding 10 3 0.400 None 0 1
CUI: C0038002
Disease: Splenomegaly
Splenomegaly 		phenotype Pathological Conditions, Signs and Symptoms Finding 345 19 0.100 None 0
CUI: C0019214
Disease: Hepatosplenomegaly
Hepatosplenomegaly 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Hemic and Lymphatic Diseases Sign or Symptom 127 21 0.100 None 0
CUI: C0028081
Disease: Night sweats
Night sweats 		phenotype Sign or Symptom 17 0.100 None 0
CUI: C0019618
Disease: Histiocytosis
Histiocytosis 		disease Hemic and Lymphatic Diseases Neoplastic Process 32 3 0.100 None 0
CUI: C1856920
Disease: Hypoplasia of the femoral head
Hypoplasia of the femoral head 		phenotype Finding 4 0.100 None 0
CUI: C0023518
Disease: Leukocytosis
Leukocytosis 		phenotype Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 168 4 0.100 None 0
CUI: C2930924
Disease: Interferon gamma, receptor 1, deficiency
Interferon gamma, receptor 1, deficiency 		disease Infections Disease or Syndrome 2 0.300 None 0
CUI: C0235896
Disease: Pulmonary Infiltrate
Pulmonary Infiltrate 		phenotype Respiratory Tract Diseases Finding 43 0.100 None 0
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes 		group Immune System Diseases Disease or Syndrome 973 31 0.100 None 0
CUI: C0836924
Disease: Thrombocytosis
Thrombocytosis 		disease Hemic and Lymphatic Diseases Disease or Syndrome 93 12 0.100 None 0
CUI: C0497156
Disease: Lymphadenopathy
Lymphadenopathy 		phenotype Hemic and Lymphatic Diseases Disease or Syndrome 277 5 0.100 None 0
CUI: C0002871
Disease: Anemia
Anemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 847 94 0.100 None 0
CUI: C0003123
Disease: Anorexia
Anorexia 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 242 10 0.100 None 0
CUI: C0476486
Disease: Generalized enlarged lymph nodes
Generalized enlarged lymph nodes 		disease Hemic and Lymphatic Diseases Disease or Syndrome 13 0.100 None 0
CUI: C4476771
Disease: Abnormal bronchus physiology
Abnormal bronchus physiology 		phenotype Finding 1 0.100 None 0