RARA, retinoic acid receptor alpha, 5914

N. diseases: 274; N. variants: 3
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: C4023031
Disease: Abnormal granulocytopoietic cell morphology
Abnormal granulocytopoietic cell morphology 		disease Finding 2 0.100 None 0
CUI: C0242013
Disease: Sciatic Neuritis
Sciatic Neuritis 		disease Nervous System Diseases Disease or Syndrome 4 0.300 None 1.000 1 2006 2006
CUI: C0751924
Disease: Neuralgia-Neuritis, Sciatic Nerve
Neuralgia-Neuritis, Sciatic Nerve 		disease Nervous System Diseases Disease or Syndrome 4 0.300 None 1.000 1 2006 2006
CUI: C0751925
Disease: Sciatic Nerve Palsy
Sciatic Nerve Palsy 		disease Nervous System Diseases Disease or Syndrome 4 0.300 None 1.000 1 2006 2006
CUI: C2854122
Disease: Acute myeloblastic leukemia with t(8;21)
Acute myeloblastic leukemia with t(8;21) 		disease Neoplastic Process 4 0.010 None 1.000 1 1999 1999
CUI: C0086696
Disease: Neoplasms, Therapy-Associated
Neoplasms, Therapy-Associated 		phenotype Neoplasms Neoplastic Process 6 0.300 None 1.000 1 2010 2010
CUI: C3266843
Disease: 47, XYY syndrome
47, XYY syndrome 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 9 0.010 None 1.000 1 2014 2014
CUI: C0154748
Disease: Lesion of Sciatic Nerve
Lesion of Sciatic Nerve 		disease Nervous System Diseases Disease or Syndrome 11 0.300 None 1.000 1 2006 2006
CUI: C3805089
Disease: Hyperfibrinolysis
Hyperfibrinolysis 		disease Hemic and Lymphatic Diseases Disease or Syndrome 12 0.010 None 1.000 1 2017 2017
CUI: C0022584
Disease: Keratoderma, Palmoplantar, Diffuse
Keratoderma, Palmoplantar, Diffuse 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 13 1 0.010 None 1.000 1 1993 1993
CUI: C0877578
Disease: Treatment related secondary malignancy
Treatment related secondary malignancy 		disease Neoplasms Neoplastic Process 13 0.300 None 1.000 1 2010 2010
CUI: C0600066
Disease: Malignant Cystosarcoma Phyllodes
Malignant Cystosarcoma Phyllodes 		disease Neoplasms Neoplastic Process 16 0.300 None 1.000 1 2015 2015
CUI: C4324477
Disease: Transformation to acute myeloid leukaemia
Transformation to acute myeloid leukaemia 		disease Neoplasms Neoplastic Process 16 0.010 None 1.000 1 2014 2014
CUI: C0025874
Disease: Metrorrhagia
Metrorrhagia 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Pathologic Function 17 2 0.100 None 0
CUI: C0239134
Disease: Productive Cough
Productive Cough 		phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Finding 17 0.100 None 0
CUI: C4552938
Disease: Productive Cough, CTCAE
Productive Cough, CTCAE 		phenotype Finding 17 0.100 None 0
CUI: C4022608
Disease: Oral cavity bleeding
Oral cavity bleeding 		phenotype Pathologic Function 18 0.100 None 0
CUI: C4324336
Disease: Hyperleukocytosis
Hyperleukocytosis 		disease Disease or Syndrome 21 0.010 None 1.000 1 2001 2001
CUI: C4476767
Disease: Diffuse alveolar hemorrhage
Diffuse alveolar hemorrhage 		disease Disease or Syndrome 21 0.100 None 0
CUI: C0019112
Disease: Hemorrhoids
Hemorrhoids 		disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 24 0.010 None 1.000 1 2019 2019
CUI: C1836653
Disease: Ascending aortic dissection
Ascending aortic dissection 		phenotype Cardiovascular Diseases Disease or Syndrome 25 1 0.010 None 1.000 1 2017 2017
CUI: C1860320
Disease: Bone marrow hypercellularity
Bone marrow hypercellularity 		phenotype Finding 26 0.100 None 0
CUI: C1619700
Disease: RENAL ADYSPLASIA
RENAL ADYSPLASIA 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Congenital Abnormality 29 6 0.010 None 1.000 1 2017 2017
CUI: C4721505
Disease: Sarcoma, Myeloid
Sarcoma, Myeloid 		disease Neoplasms Neoplastic Process 31 1 0.020 None 1.000 2 2010 2015
CUI: C0542519
Disease: Congenital absence of kidney
Congenital absence of kidney 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Congenital Abnormality 33 3 0.010 None 1.000 1 2017 2017