MIA, MIA SH3 domain containing, 8190

N. diseases: 130; 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.
Multiple gastrointestinal atresias (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 5 23 0.020 None 1.000 2 2011 2018
Undifferentiated Pancreatic Carcinoma
disease Neoplastic Process 7 0.010 None 1.000 1 2000 2000
CUI: C0015814
Disease: Femur Head Necrosis
Femur Head Necrosis
disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Disease or Syndrome 8 0.200 None 1.000 1 2010 2010
CUI: C0032371
Disease: Poliomyelitis
Poliomyelitis
disease Infections; Nervous System Diseases Disease or Syndrome 23 0.010 None 1.000 1 2017 2017
CUI: C0262929
Disease: Myxoma of the Endocardium
Myxoma of the Endocardium
disease Neoplasms Neoplastic Process 28 0.010 None 1.000 1 2004 2004
CUI: C3149631
Disease: MELORHEOSTOSIS, ISOLATED
MELORHEOSTOSIS, ISOLATED
disease Disease or Syndrome 35 0.010 None 1.000 1 2013 2013
CUI: C4049711
Disease: Lepidic Predominant Adenocarcinoma
Lepidic Predominant Adenocarcinoma
disease Neoplasms Neoplastic Process 46 0.010 None 1.000 1 2016 2016
Intraductal papillary mucinous neoplasm
disease Neoplastic Process 50 2 0.010 None 1.000 1 2019 2019
CUI: C1527358
Disease: Phototoxicity
Phototoxicity
disease Skin and Connective Tissue Diseases Disease or Syndrome 52 0.010 None 1.000 1 2018 2018
CUI: C0334276
Disease: Adenocarcinoma in Situ
Adenocarcinoma in Situ
phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 55 0.010 None 1.000 1 2018 2018
CUI: C0206093
Disease: Neuroectodermal Tumors
Neuroectodermal Tumors
disease Neoplasms Neoplastic Process 56 0.010 None 1.000 1 1994 1994
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 74 68 0.010 None 1.000 1 2017 2017
Pancreatic Intraductal Papillary Mucinous Neoplasm
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 84 8 0.010 None 1.000 1 2019 2019
CUI: C0162830
Disease: Dermatitis, Phototoxic
Dermatitis, Phototoxic
disease Skin and Connective Tissue Diseases Disease or Syndrome 89 0.010 None 1.000 1 2018 2018
CUI: C3665593
Disease: Melanocytic nevus of skin
Melanocytic nevus of skin
disease Neoplasms Neoplastic Process 103 3 0.010 None 1.000 1 1999 1999
CUI: C0393591
Disease: AICARDI-GOUTIERES SYNDROME
AICARDI-GOUTIERES SYNDROME
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Nervous System Diseases Disease or Syndrome 117 12 0.010 None 1.000 1 2002 2002
CUI: C0677944
Disease: Sentinel node (disorder)
Sentinel node (disorder)
disease Disease or Syndrome 130 5 0.010 None 1.000 1 2004 2004
CUI: C0007120
Disease: Bronchioloalveolar Adenocarcinoma
Bronchioloalveolar Adenocarcinoma
disease Neoplasms Neoplastic Process 136 5 0.010 None 1.000 1 2016 2016
CUI: C0020437
Disease: Hypercalcemia
Hypercalcemia
disease Nutritional and Metabolic Diseases Disease or Syndrome 157 9 0.010 None 1.000 1 1991 1991
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms
group Neoplasms; Nervous System Diseases Neoplastic Process 180 72 0.010 None < 0.001 1 2002 2002
CUI: C0033036
Disease: Atrial Premature Complexes
Atrial Premature Complexes
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 183 21 0.010 None 1.000 1 2017 2017
CUI: C0563625
Disease: Agnosia for Pain
Agnosia for Pain
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 204 25 0.010 None 1.000 1 2017 2017
CUI: C3714948
Disease: PACHYONYCHIA CONGENITA 3
PACHYONYCHIA CONGENITA 3
disease Disease or Syndrome 209 20 0.010 None 1.000 1 2017 2017
CUI: C4282128
Disease: PATENT DUCTUS ARTERIOSUS 1
PATENT DUCTUS ARTERIOSUS 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 229 12 0.010 None 1.000 1 2017 2017
CUI: C0085110
Disease: Severe Combined Immunodeficiency
Severe Combined Immunodeficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases Disease or Syndrome 284 46 0.020 None 1.000 2 2011 2011