HTRA2, HtrA serine peptidase 2, 27429

N. diseases: 151; N. variants: 6
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.
3-METHYLGLUTACONIC ACIDURIA, TYPE VIII
disease Disease or Syndrome 1 1 0.600 None 1.000 4 1 2005 2017
PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO
disease Finding 1 2 0.700 limited 1.000 3 2 2005 2013
CUI: C0393615
Disease: Familial Tremor
Familial Tremor
disease Nervous System Diseases Disease or Syndrome 5 1 0.010 None 1.000 1 1 2014 2014
Autosomal dominant late onset Parkinson disease
disease Nervous System Diseases Disease or Syndrome 9 5 0.010 None 1.000 1 2018 2018
Posterior Circulation Transient Ischemic Attack
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2004 2004
Carotid Circulation Transient Ischemic Attack
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2004 2004
Transient Ischemic Attack, Vertebrobasilar Circulation
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2004 2004
Crescendo Transient Ischemic Attacks
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2004 2004
CUI: C0751022
Disease: Brain Stem Ischemia, Transient
Brain Stem Ischemia, Transient
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2004 2004
Transient Ischemic Attack, Anterior Circulation
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2004 2004
CUI: C0278097
Disease: Abnormal male sexual function
Abnormal male sexual function
disease Mental or Behavioral Dysfunction 12 0.100 None 0
CUI: C1112443
Disease: Male sexual dysfunction
Male sexual dysfunction
disease Disease or Syndrome 12 0.100 None 0
CUI: C3696376
Disease: 3-Methylglutaconic Aciduria
3-Methylglutaconic Aciduria
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 20 1 0.130 None 1.000 3 2016 2018
CUI: C0338455
Disease: Dementia of frontal lobe type
Dementia of frontal lobe type
disease Nervous System Diseases; Mental Disorders Disease or Syndrome 20 0.100 None 0
Parkinsonism with favorable response to dopaminergic medication
phenotype Nervous System Diseases Finding 21 2 0.100 None 0
CUI: C1112442
Disease: Female sexual dysfunction
Female sexual dysfunction
disease Mental or Behavioral Dysfunction 22 3 0.100 None 0
CUI: C0242423
Disease: Ramsay Hunt Paralysis Syndrome
Ramsay Hunt Paralysis Syndrome
disease Nervous System Diseases Disease or Syndrome 28 0.300 None 1.000 1 2015 2015
Autosomal Dominant Juvenile Parkinson Disease
disease Nervous System Diseases Disease or Syndrome 28 0.300 None 1.000 1 2015 2015
CUI: C0752101
Disease: Parkinsonism, Experimental
Parkinsonism, Experimental
disease Nervous System Diseases Experimental Model of Disease 28 0.300 None 1.000 1 2015 2015
CUI: C0752104
Disease: Familial Juvenile Parkinsonism
Familial Juvenile Parkinsonism
disease Nervous System Diseases Disease or Syndrome 28 0.300 None 1.000 1 2015 2015
CUI: C0752100
Disease: Autosomal Recessive Parkinsonism
Autosomal Recessive Parkinsonism
disease Nervous System Diseases Disease or Syndrome 33 1 0.300 None 1.000 1 2015 2015
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
Autosomal Dominant Parkinsonism
disease Nervous System Diseases Disease or Syndrome 34 3 0.300 None 1.000 1 2015 2015
CUI: C0752105
Disease: Parkinsonism, Juvenile
Parkinsonism, Juvenile
disease Nervous System Diseases Disease or Syndrome 40 2 0.300 None 1.000 1 2015 2015
CUI: C0150080
Disease: Social Communication Disorder
Social Communication Disorder
disease Mental Disorders Mental or Behavioral Dysfunction 40 4 0.100 None 0
CUI: C0004045
Disease: Asphyxia Neonatorum
Asphyxia Neonatorum
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 45 5 0.200 None 1.000 1 2010 2010