Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: |
HP:0010525 | HP:0010525 | Finger agnosia | 0 | ABCA7 CL E G H | 10347 | 37 | ORPHA:1020 | Early-onset autosomal dominant Alzheimer disease | HP:0040283 - Occasional | | | 3 | | |
HP:0010525 | HP:0010525 | Finger agnosia | 0 | APP CL E G H | 351 | 620 | ORPHA:1020 | Early-onset autosomal dominant Alzheimer disease | HP:0040283 - Occasional | | | 74 | | |
HP:0010525 | HP:0010525 | Finger agnosia | 0 | PSEN1 CL E G H | 5663 | 9508 | ORPHA:1020 | Early-onset autosomal dominant Alzheimer disease | HP:0040283 - Occasional | | | 241 | | |
HP:0010525 | HP:0010525 | Finger agnosia | 0 | PSEN2 CL E G H | 5664 | 9509 | ORPHA:1020 | Early-onset autosomal dominant Alzheimer disease | HP:0040283 - Occasional | | | 59 | | |
HP:0010525 | HP:0010525 | Finger agnosia | 0 | SORL1 CL E G H | 6653 | 11185 | ORPHA:1020 | Early-onset autosomal dominant Alzheimer disease | HP:0040283 - Occasional | | | 3 | | |
HP:0010525 | HP:0010525 | Finger agnosia | 0 | TOMM40 CL E G H | 10452 | 18001 | ORPHA:1020 | Early-onset autosomal dominant Alzheimer disease | HP:0040283 - Occasional | | | | | |
HP:0010525 | HP:0010525 | Finger agnosia | 0 | TREM2 CL E G H | 54209 | 17761 | ORPHA:1020 | Early-onset autosomal dominant Alzheimer disease | HP:0040283 - Occasional | | | 31 | | |