HTRA1, HtrA serine peptidase 1, 5654

N. diseases: 164; N. variants: 45
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1838577
Disease: Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C1838577
Disease: Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C1838577
Disease: Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 		0.800 Biomarker disease CTD_human
CUI: C4225211
Disease: CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C4225211
Disease: CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2 		0.600 GeneticVariation disease CLINVAR
CUI: C4225211
Disease: CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2 		0.600 CausalMutation disease CLINVAR
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.500 Biomarker disease GENOMICS_ENGLAND
CUI: C2733158
Disease: Cerebral Small Vessel Diseases
Cerebral Small Vessel Diseases 		0.500 GeneticVariation group CLINVAR
CUI: C0002170
Disease: Alopecia
Alopecia 		0.410 Biomarker disease HPO
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.410 GeneticVariation disease CLINVAR
CUI: C0497327
Disease: Dementia
Dementia 		0.400 Biomarker disease HPO
CUI: C0497327
Disease: Dementia
Dementia 		0.400 Biomarker disease GENOMICS_ENGLAND
CUI: C1857813
Disease: Macular Degeneration, Age-Related, 7
Macular Degeneration, Age-Related, 7 		0.400 SusceptibilityMutation disease CLINVAR
CUI: C1857813
Disease: Macular Degeneration, Age-Related, 7
Macular Degeneration, Age-Related, 7 		0.400 Biomarker disease CTD_human
CUI: C0751587
Disease: CADASIL Syndrome
CADASIL Syndrome 		0.340 Biomarker disease CTD_human
CUI: C0026654
Disease: Moyamoya Disease
Moyamoya Disease 		0.300 Biomarker disease GENOMICS_ENGLAND
CUI: C1449626
Disease: CADASILM
CADASILM 		0.300 Biomarker disease CTD_human
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.110 Biomarker group HPO
CUI: C0234985
Disease: Mental deterioration
Mental deterioration 		0.110 Biomarker phenotype HPO
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy 		0.110 Biomarker group HPO
CUI: C0004134
Disease: Ataxia
Ataxia 		0.100 Biomarker phenotype HPO
CUI: C0007787
Disease: Transient Ischemic Attack
Transient Ischemic Attack 		0.100 Biomarker disease HPO
CUI: C0013362
Disease: Dysarthria
Dysarthria 		0.100 Biomarker disease HPO
CUI: C0018681
Disease: Headache
Headache 		0.100 Biomarker phenotype HPO
CUI: C0024031
Disease: Low Back Pain
Low Back Pain 		0.100 Biomarker phenotype HPO