MIR221, microRNA 221, 407006

N. diseases: 288; N. variants: 2
Source: BEFREE ×
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: C4330601
Disease: MGMT-Unmethylated Glioblastoma
MGMT-Unmethylated Glioblastoma 		disease Neoplasms Neoplastic Process 2 0.010 None 1.000 1 2018 2018
CUI: C4544197
Disease: Acute obstructive cholangitis
Acute obstructive cholangitis 		disease Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C1266132
Disease: Metastasizing leiomyoma
Metastasizing leiomyoma 		disease Neoplasms; Musculoskeletal Diseases Neoplastic Process 4 0.010 None 1.000 1 2008 2008
CUI: C0265255
Disease: Trichorhinophalangeal syndrome
Trichorhinophalangeal syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases Disease or Syndrome 6 1 0.010 None 1.000 1 2011 2011
CUI: C3494609
Disease: Asymptomatic carotid artery stenosis
Asymptomatic carotid artery stenosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 6 0.010 None 1.000 1 2017 2017
CUI: C0340364
Disease: Familial mitral valve prolapse
Familial mitral valve prolapse 		disease Cardiovascular Diseases Congenital Abnormality 9 0.010 None 1.000 1 2019 2019
CUI: C0277527
Disease: Epidemic diarrhea
Epidemic diarrhea 		disease Digestive System Diseases; Infections Disease or Syndrome 19 0.010 None 1.000 1 2018 2018
CUI: C1335475
Disease: Primary Carcinoma
Primary Carcinoma 		phenotype Neoplasms Neoplastic Process 25 2 0.010 None 1.000 1 2010 2010
CUI: C0158288
Disease: Spinal stenosis of lumbar region
Spinal stenosis of lumbar region 		disease Musculoskeletal Diseases Disease or Syndrome 32 0.010 None 1.000 1 2016 2016
CUI: C0752130
Disease: Spinal Cord Ischemia
Spinal Cord Ischemia 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 33 3 0.010 None 1.000 1 2018 2018
CUI: C1851100
Disease: LAURIN-SANDROW SYNDROME
LAURIN-SANDROW SYNDROME 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 35 0.010 None 1.000 1 2016 2016
CUI: C2986561
Disease: Spindle Cell Oncocytoma of the Adenohypophysis
Spindle Cell Oncocytoma of the Adenohypophysis 		disease Neoplasms Neoplastic Process 35 2 0.010 None 1.000 1 2017 2017
CUI: C0240225
Disease: Liver mass
Liver mass 		phenotype Disease or Syndrome 36 0.010 None 1.000 1 2017 2017
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 38 2 0.010 None 1.000 1 2010 2010
CUI: C0010418
Disease: Cryptosporidiosis
Cryptosporidiosis 		disease Digestive System Diseases; Infections; Animal Diseases Disease or Syndrome 40 0.010 None 1.000 1 2011 2011
CUI: C2882221
Disease: Acute pulmonary embolism
Acute pulmonary embolism 		disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 42 0.010 None 1.000 1 2018 2018
CUI: C0027654
Disease: Embryonal Neoplasm
Embryonal Neoplasm 		disease Neoplasms Neoplastic Process 43 2 0.010 None 1.000 1 2014 2014
CUI: C1709457
Disease: Papillary Thyroid Microcarcinoma
Papillary Thyroid Microcarcinoma 		disease Neoplasms; Endocrine System Diseases Neoplastic Process 46 2 0.010 None 1.000 1 2018 2018
CUI: C3163918
Disease: Tumor thrombus
Tumor thrombus 		phenotype Cardiovascular Diseases Disease or Syndrome 50 3 0.010 None 1.000 1 2014 2014
CUI: C4551538
Disease: refractory multiple myeloma
refractory multiple myeloma 		disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process 50 1 0.010 None 1.000 1 2016 2016
CUI: C0878773
Disease: Overactive Bladder
Overactive Bladder 		disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 57 3 0.010 None 1.000 1 2018 2018
CUI: C0279613
Disease: Childhood Alveolar Rhabdomyosarcoma
Childhood Alveolar Rhabdomyosarcoma 		disease Neoplasms Neoplastic Process 59 0.010 None 1.000 1 2018 2018
CUI: C1839780
Disease: FRAGILE X TREMOR/ATAXIA SYNDROME
FRAGILE X TREMOR/ATAXIA SYNDROME 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 62 0.010 None 1.000 1 2013 2013
CUI: C0018572
Disease: Hand, Foot and Mouth Disease
Hand, Foot and Mouth Disease 		disease Infections Disease or Syndrome 63 13 0.010 None 1.000 1 2018 2018
CUI: C0085293
Disease: Hepatitis E
Hepatitis E 		disease Digestive System Diseases; Infections Disease or Syndrome 69 2 0.010 None 1.000 1 2013 2013