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:0010522 | HP:0010522 | Dyslexia | 0 | APC CL E G H | 324 | 583 | ORPHA:261584 | Familial adenomatous polyposis due to 5q22.2 microdeletion | HP:0040282 - Frequent | | | 3179 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | C9ORF72 CL E G H | 203228 | 28337 | ORPHA:275864 | Behavioral variant of frontotemporal dementia | HP:0040281 - Very frequent | | | 56 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | C9ORF72 CL E G H | 203228 | 28337 | ORPHA:100069 | Semantic dementia | HP:0040282 - Frequent | | | 56 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | CACNA1H CL E G H | 8912 | 1395 | ORPHA:64280 | Childhood absence epilepsy | HP:0040283 - Occasional | | | 75 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | CHMP2B CL E G H | 25978 | 24537 | ORPHA:275864 | Behavioral variant of frontotemporal dementia | HP:0040281 - Very frequent | | | 42 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | CHMP2B CL E G H | 25978 | 24537 | ORPHA:100069 | Semantic dementia | HP:0040282 - Frequent | | | 42 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | DNAAF4 CL E G H | 161582 | 21493 | OMIM:127700 | Dyslexia, susceptibility to, 1 | . | | | 27 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | FRMD5 CL E G H | 84978 | 28214 | OMIM:620094 | | | | | | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | GABRA1 CL E G H | 2554 | 4075 | ORPHA:64280 | Childhood absence epilepsy | HP:0040283 - Occasional | | | 134 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | GABRB3 CL E G H | 2562 | 4083 | ORPHA:64280 | Childhood absence epilepsy | HP:0040283 - Occasional | | | 57 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | GABRG2 CL E G H | 2566 | 4087 | ORPHA:64280 | Childhood absence epilepsy | HP:0040283 - Occasional | | | 139 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | GCLC CL E G H | 2729 | 4311 | ORPHA:33574 | Glutamate-cysteine ligase deficiency | HP:0040283 - Occasional | | | 2 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | GRN CL E G H | 2896 | 4601 | ORPHA:275864 | Behavioral variant of frontotemporal dementia | HP:0040281 - Very frequent | | | 126 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | GRN CL E G H | 2896 | 4601 | ORPHA:100069 | Semantic dementia | HP:0040282 - Frequent | | | 126 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | JRK CL E G H | 8629 | 6199 | ORPHA:64280 | Childhood absence epilepsy | HP:0040283 - Occasional | | | | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | MAP1B CL E G H | 4131 | 6836 | OMIM:618918 | PERIVENTRICULAR NODULAR HETEROTOPIA 9; PVNH9 | | | | | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | MAPT CL E G H | 4137 | 6893 | ORPHA:275864 | Behavioral variant of frontotemporal dementia | HP:0040281 - Very frequent | | | 140 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | MAPT CL E G H | 4137 | 6893 | ORPHA:100069 | Semantic dementia | HP:0040282 - Frequent | | | 140 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | NIPA1 CL E G H | 123606 | 17043 | ORPHA:261183 | 15q11.2 microdeletion syndrome | HP:0040282 - Frequent | | | 117 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | NIPA2 CL E G H | 81614 | 17044 | ORPHA:261183 | 15q11.2 microdeletion syndrome | HP:0040282 - Frequent | | | 1 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | OPA3 CL E G H | 80207 | 8142 | ORPHA:67036 | Autosomal dominant optic atrophy and cataract | HP:0040283 - Occasional | | | 163 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | PLA2G6 CL E G H | 8398 | 9039 | ORPHA:199351 | Adult-onset dystonia-parkinsonism | HP:0040282 - Frequent | | | 133 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | PNKP CL E G H | 11284 | 9154 | ORPHA:459033 | Ataxia-oculomotor apraxia type 4 | HP:0040283 - Occasional | | | 244 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | PSEN1 CL E G H | 5663 | 9508 | ORPHA:275864 | Behavioral variant of frontotemporal dementia | HP:0040281 - Very frequent | | | 241 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | PSEN1 CL E G H | 5663 | 9508 | ORPHA:100069 | Semantic dementia | HP:0040282 - Frequent | | | 241 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | SARDH CL E G H | 1757 | 10536 | ORPHA:3129 | Sarcosinemia | HP:0040283 - Occasional | | | 4 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | SLC2A1 CL E G H | 6513 | 11005 | ORPHA:64280 | Childhood absence epilepsy | HP:0040283 - Occasional | | | 255 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | SPTBN1 CL E G H | 6711 | 11275 | OMIM:619475 | DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES; DDISBA | | | | | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | SQSTM1 CL E G H | 8878 | 11280 | ORPHA:275864 | Behavioral variant of frontotemporal dementia | HP:0040281 - Very frequent | | | 62 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | STIM1 CL E G H | 6786 | 11386 | OMIM:185070 | Stormorken syndrome | . | | | 31 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | TCF12 CL E G H | 6938 | 11623 | OMIM:619718 | HYPOGONADOTROPIC HYPOGONADISM 26 WITH OR WITHOUT ANOSMIA; HH26 | | | | 28 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | TMEM106B CL E G H | 54664 | 22407 | ORPHA:275864 | Behavioral variant of frontotemporal dementia | HP:0040281 - Very frequent | | | | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | TMEM106B CL E G H | 54664 | 22407 | ORPHA:100069 | Semantic dementia | HP:0040282 - Frequent | | | | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | TREM2 CL E G H | 54209 | 17761 | ORPHA:275864 | Behavioral variant of frontotemporal dementia | HP:0040281 - Very frequent | | | 31 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | TREM2 CL E G H | 54209 | 17761 | ORPHA:100069 | Semantic dementia | HP:0040282 - Frequent | | | 31 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | TUBG1 CL E G H | 7283 | 12417 | ORPHA:261183 | 15q11.2 microdeletion syndrome | HP:0040282 - Frequent | | | 14 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | VCP CL E G H | 7415 | 12666 | ORPHA:275864 | Behavioral variant of frontotemporal dementia | HP:0040281 - Very frequent | | | 63 | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | VPS13D CL E G H | 55187 | 23595 | ORPHA:95434 | Autosomal recessive cerebellar ataxia-movement disorder syndrome | HP:0040282 - Frequent | | | | | |
HP:0010522 | HP:0010522 | Dyslexia | 0 | VPS41 CL E G H | 27072 | 12713 | ORPHA:95434 | Autosomal recessive cerebellar ataxia-movement disorder syndrome | HP:0040282 - Frequent | | | | | |