ERBB4, erb-b2 receptor tyrosine kinase 4, 2066

N. diseases: 317; N. variants: 75
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: C1262106
Disease: Neuromuscular toxicity
Neuromuscular toxicity
disease Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C3541908
Disease: Sperm Motility Measurement
Sperm Motility Measurement
phenotype Laboratory Procedure 1 1 0.100 None 1.000 1 1 2018 2018
CUI: C3715155
Disease: AMYOTROPHIC LATERAL SCLEROSIS 19
AMYOTROPHIC LATERAL SCLEROSIS 19
disease Disease or Syndrome 1 2 0.700 None 1.000 1 2 2013 2013
Metastatic Oral Cavity Squamous Cell Carcinoma
disease Neoplastic Process 1 0.010 None 1.000 1 2005 2005
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
disease Disease or Syndrome 4 9 0.010 None 1.000 1 2017 2017
CUI: C0428419
Disease: Triiodothyronine measurement
Triiodothyronine measurement
phenotype Laboratory Procedure 6 12 0.100 None 1.000 1 1 2019 2019
CUI: C2007076
Disease: Liver Carcinosarcoma
Liver Carcinosarcoma
disease Neoplasms Neoplastic Process 7 0.010 None 1.000 1 2019 2019
CUI: C0154742
Disease: Other lesions of median nerve
Other lesions of median nerve
phenotype Nervous System Diseases Pathologic Function 8 0.200 None 1.000 1 2009 2009
CUI: C0270855
Disease: Early myoclonic encephalopathy
Early myoclonic encephalopathy
disease Nervous System Diseases Disease or Syndrome 10 7 0.020 None 1.000 2 2009 2012
Left ventricular outflow tract obstruction
disease Congenital Abnormality 13 2 0.010 None 1.000 1 2011 2011
CUI: C2112532
Disease: Postmenopausal endometrium
Postmenopausal endometrium
disease Disease or Syndrome 15 0.010 None 1.000 1 2007 2007
CUI: C0392702
Disease: Abnormal involuntary movement
Abnormal involuntary movement
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 22 10 0.010 None 1.000 1 2019 2019
CUI: C1142339
Disease: Intestinal adenoma
Intestinal adenoma
disease Neoplastic Process 23 0.010 None 1.000 1 2016 2016
CUI: C0202231
Disease: Thyroxine measurement
Thyroxine measurement
phenotype Laboratory Procedure 24 42 0.100 None 1.000 1 1 2019 2019
CUI: C0700594
Disease: Radiculopathy
Radiculopathy
disease Nervous System Diseases Disease or Syndrome 25 0.200 None 1.000 1 2006 2006
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
disease Disease or Syndrome 27 67 0.100 None 1.000 1 1 2014 2014
CUI: C4543929
Disease: Primary osteosarcoma
Primary osteosarcoma
disease Neoplasms Neoplastic Process 28 0.010 None 1.000 1 2004 2004
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
disease Disease or Syndrome 31 54 0.100 None 1.000 1 1 2014 2014
CUI: C0523677
Disease: Glycine measurement
Glycine measurement
phenotype Laboratory Procedure 32 68 0.100 None 1.000 1 1 2019 2019
HMN (Hereditary Motor Neuropathy) Proximal Type I
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 34 8 0.010 None 1.000 1 2016 2016
CUI: C0346255
Disease: Oncocytoma, renal
Oncocytoma, renal
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 34 0.010 None 1.000 1 2018 2018
T-Cell Large Granular Lymphocyte Leukemia
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 35 4 0.010 None 1.000 1 2014 2014
CUI: C0262401
Disease: Carcinoma of ampulla of Vater
Carcinoma of ampulla of Vater
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 37 4 0.010 None 1.000 1 2018 2018
CUI: C4551854
Disease: HYPOPLASTIC LEFT HEART SYNDROME 1
HYPOPLASTIC LEFT HEART SYNDROME 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 37 12 0.010 None 1.000 1 2011 2011
CUI: C1849097
Disease: Loss of ability to walk
Loss of ability to walk
phenotype Finding 37 11 0.100 None 0