APP, amyloid beta precursor protein, 351

N. diseases: 485; N. variants: 114
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia
0.100 Biomarker phenotype HPO
CUI: C0030554
Disease: Paresthesia
Paresthesia
0.100 Biomarker phenotype HPO
Neurofibrillary degeneration (morphologic abnormality)
0.100 Biomarker phenotype HPO
CUI: C0085631
Disease: Agitation
Agitation
0.100 Biomarker phenotype HPO
CUI: C0149854
Disease: Cerebellar hemorrhage
Cerebellar hemorrhage
0.100 Biomarker phenotype HPO
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.100 Biomarker group HPO
CUI: C0234144
Disease: Dysgraphia
Dysgraphia
0.100 Biomarker disease HPO
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition
0.100 Biomarker phenotype HPO
CUI: C0234509
Disease: Finger Agnosia
Finger Agnosia
0.100 Biomarker phenotype HPO
CUI: C0270685
Disease: Cerebral calcification
Cerebral calcification
0.100 Biomarker phenotype HPO
CUI: C0271270
Disease: Oculovestibuloauditory syndrome
Oculovestibuloauditory syndrome
0.100 Biomarker disease HPO
CUI: C0338462
Disease: Semantic Dementia
Semantic Dementia
0.100 Biomarker disease HPO
CUI: C0424296
Disease: Social disinhibition
Social disinhibition
0.100 Biomarker disease HPO
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
0.100 Biomarker disease HPO
CUI: C0575081
Disease: Gait abnormality
Gait abnormality
0.100 Biomarker group HPO
CUI: C0917798
Disease: Cerebral Ischemia
Cerebral Ischemia
0.100 Biomarker disease HPO
CUI: C1836791
Disease: Tortuous cerebral arteries
Tortuous cerebral arteries
0.100 Biomarker phenotype HPO
Deposits immunoreactive to beta-amyloid protein
0.100 Biomarker phenotype HPO
CUI: C1865903
Disease: Long-tract signs
Long-tract signs
0.100 Biomarker phenotype HPO
CUI: C1963060
Disease: Agitation, CTCAE 3.0
Agitation, CTCAE 3.0
0.100 Biomarker phenotype HPO
CUI: C1963167
Disease: Memory Impairment, CTCAE 3.0
Memory Impairment, CTCAE 3.0
0.100 Biomarker phenotype HPO
CUI: C2931257
Disease: Alzheimer disease type 1
Alzheimer disease type 1
0.100 CausalMutation disease CLINVAR
CUI: C3489733
Disease: Oculomotor apraxia
Oculomotor apraxia
0.100 Biomarker disease HPO
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT
0.100 CausalMutation phenotype CLINVAR
CUI: C4021087
Disease: Abnormal social behavior
Abnormal social behavior
0.100 Biomarker phenotype HPO