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:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | ABCD1 CL E G H | 215 | 61 | ORPHA:139399 | Adrenomyeloneuropathy | | | | 135 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | AIFM1 CL E G H | 9131 | 8768 | ORPHA:83629 | Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome | HP:0040282 - Frequent | | | 60 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | ALS2 CL E G H | 57679 | 443 | OMIM:607225 | Spastic paralysis, infantile-onset ascending | | | | 114 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | ATL1 CL E G H | 51062 | 11231 | OMIM:182600 | Spastic paraplegia 3, autosomal dominant | | | | 71 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | ATP1A2 CL E G H | 477 | 800 | OMIM:619602 | FETAL AKINESIA, RESPIRATORY INSUFFICIENCY, MICROCEPHALY, POLYMICROGYRIA, AND DYSMORPHIC FACIES; FARIMPD | | | | 239 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | ATP6 CL E G H | 4508 | 7414 | ORPHA:644 | NARP syndrome | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | ATP6 CL E G H | 4508 | 7414 | OMIM:551500 | Neuropathy, ataxia, and retinitis pigmentosa | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | ATXN10 CL E G H | 25814 | 10549 | OMIM:603516 | Spinocerebellar ataxia 10 | . | | | 9 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | ATXN8 CL E G H | 724066 | 32925 | OMIM:608768 | Spinocerebellar ataxia 8 | . | | | 1 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | ATXN8OS CL E G H | 6315 | 10561 | OMIM:608768 | Spinocerebellar ataxia 8 | . | | | 1 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | BAZ1B CL E G H | 9031 | 961 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | BCL7B CL E G H | 9275 | 1005 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | BUD23 CL E G H | 114049 | 16405 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | C9ORF72 CL E G H | 203228 | 28337 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 56 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | CHCHD10 CL E G H | 400916 | 15559 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 11 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | CLIP2 CL E G H | 7461 | 2586 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | CPT1C CL E G H | 126129 | 18540 | ORPHA:444099 | Autosomal dominant spastic paraplegia type 73 | | | | 1 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | CTC1 CL E G H | 80169 | 26169 | OMIM:612199 | Cerebroretinal microangiopathy with calcifications and cysts | . | | | 160 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | DCC CL E G H | 1630 | 2701 | ORPHA:238722 | Familial congenital mirror movements | | | | 36 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | DCTN1 CL E G H | 1639 | 2711 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | | | | 86 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | DEAF1 CL E G H | 10522 | 14677 | ORPHA:819 | Smith-Magenis syndrome | | | | 33 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | DNAJC30 CL E G H | 84277 | 16410 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | DNAL4 CL E G H | 10126 | 2955 | ORPHA:238722 | Familial congenital mirror movements | | | | 2 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | DPYS CL E G H | 1807 | 3013 | OMIM:222748 | Dihydropyrimidinuria | . | | | 44 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | EIF4H CL E G H | 7458 | 12741 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | ELN CL E G H | 2006 | 3327 | ORPHA:904 | Williams syndrome | | | | 172 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | FKBP6 CL E G H | 8468 | 3722 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | FKTN CL E G H | 2218 | 3622 | OMIM:253800 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 | | | | 184 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | FLII CL E G H | 2314 | 3750 | ORPHA:819 | Smith-Magenis syndrome | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | FUS CL E G H | 2521 | 4010 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 105 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | GALC CL E G H | 2581 | 4115 | ORPHA:206448 | Adult Krabbe disease | HP:0040283 - Occasional | | | 160 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | GAN CL E G H | 8139 | 4137 | OMIM:256850 | Giant axonal neuropathy 1, autosomal recessive | . | | | 121 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | GTF2I CL E G H | 2969 | 4659 | ORPHA:904 | Williams syndrome | | | | 1 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | GTF2IRD1 CL E G H | 9569 | 4661 | ORPHA:904 | Williams syndrome | | | | 1 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | GTF2IRD2 CL E G H | 84163 | 30775 | ORPHA:904 | Williams syndrome | | | | 1 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | IQSEC2 CL E G H | 23096 | 29059 | ORPHA:819 | Smith-Magenis syndrome | | | | 119 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | KCNC3 CL E G H | 3748 | 6235 | OMIM:605259 | Spinocerebellar ataxia 13 | . | | | 17 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | KPNA3 CL E G H | 3839 | 6396 | ORPHA:171612 | Autosomal dominant spastic paraplegia type 37 | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | L1CAM CL E G H | 3897 | 6470 | OMIM:307000 | Hydrocephalus due to congenital stenosis of aqueduct of sylvius | | | | 134 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | L2HGDH CL E G H | 79944 | 20499 | OMIM:236792 | L-2-Hydroxyglutaric aciduria | . | | | 34 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | LIMK1 CL E G H | 3984 | 6613 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | MAPT CL E G H | 4137 | 6893 | OMIM:260540 | Supranuclear palsy, progressive atypical | . | | | 140 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | METTL27 CL E G H | 155368 | 19068 | ORPHA:904 | Williams syndrome | | | | 1 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | MLXIPL CL E G H | 51085 | 12744 | ORPHA:904 | Williams syndrome | | | | 1 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | NCF1 CL E G H | 653361 | 7660 | ORPHA:904 | Williams syndrome | | | | 13 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | NEFH CL E G H | 4744 | 7737 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | | | | 24 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | NIPA1 CL E G H | 123606 | 17043 | OMIM:600363 | Spastic paraplegia 6, autosomal dominant | | | | 117 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | NTN1 CL E G H | 9423 | 8029 | ORPHA:238722 | Familial congenital mirror movements | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | PDHB CL E G H | 5162 | 8808 | ORPHA:255138 | Pyruvate dehydrogenase E1-beta deficiency | | | | 37 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | PLA2G6 CL E G H | 8398 | 9039 | OMIM:256600 | Neurodegeneration with brain iron accumulation 2A | . | | | 133 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | PLP1 CL E G H | 5354 | 9086 | OMIM:312920 | Spastic paraplegia 2, X-linked | | | | 60 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | PRKRA CL E G H | 8575 | 9438 | OMIM:612067 | Dystonia 16 | . | | | 37 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | PRNP CL E G H | 5621 | 9449 | ORPHA:356 | Gerstmann-Straussler-Scheinker syndrome | HP:0040282 - Frequent | | | 69 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | PRPH CL E G H | 5630 | 9461 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | | | | 25 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | RAD51 CL E G H | 5888 | 9817 | ORPHA:238722 | Familial congenital mirror movements | | | | 9 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | RAI1 CL E G H | 10743 | 9834 | ORPHA:819 | Smith-Magenis syndrome | | | | 150 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | RFC2 CL E G H | 5982 | 9970 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | RTN2 CL E G H | 6253 | 10468 | ORPHA:100993 | Autosomal dominant spastic paraplegia type 12 | | | | 25 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | SLC19A3 CL E G H | 80704 | 16266 | OMIM:607483 | Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) | . | | | 110 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | SLC25A15 CL E G H | 10166 | 10985 | OMIM:238970 | Hyperornithinemia-Hyperammonemia-Homocitrullinuria syndrome | . | | | 88 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | SLC2A1 CL E G H | 6513 | 11005 | OMIM:601042 | Dystonia 9 | . | | | 255 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | SLC33A1 CL E G H | 9197 | 95 | ORPHA:171863 | Autosomal dominant spastic paraplegia type 42 | | | | 48 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | SLC6A3 CL E G H | 6531 | 11049 | OMIM:613135 | Parkinsonism-Dystonia, infantile, 1 | . | | | 13 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | SOD1 CL E G H | 6647 | 11179 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | | | | 53 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | SPAST CL E G H | 6683 | 11233 | OMIM:182601 | Spastic paraplegia 4, autosomal dominant | | | | 208 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | SPG11 CL E G H | 80208 | 11226 | OMIM:604360 | Spastic paraplegia 11, autosomal recessive | | | | 287 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | SPG7 CL E G H | 6687 | 11237 | OMIM:607259 | Spastic paraplegia 7, autosomal recessive | | | | 171 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | SQSTM1 CL E G H | 8878 | 11280 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 62 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | STX1A CL E G H | 6804 | 11433 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | TARDBP CL E G H | 23435 | 11571 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 65 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | TBK1 CL E G H | 29110 | 11584 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 20 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | TBL2 CL E G H | 26608 | 11586 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | TMEM270 CL E G H | 135886 | 23018 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | TREX1 CL E G H | 11277 | 12269 | OMIM:225750 | Aicardi-Goutieres syndrome 1 | . | | | 56 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | UBAP1 CL E G H | 51271 | 12461 | ORPHA:100993 | Autosomal dominant spastic paraplegia type 12 | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | VAPB CL E G H | 9217 | 12649 | OMIM:608627 | Amyotrophic lateral sclerosis 8 | | | | 116 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | VCP CL E G H | 7415 | 12666 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 63 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | VPS37D CL E G H | 155382 | 18287 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | WASHC5 CL E G H | 9897 | 28984 | ORPHA:100989 | Autosomal dominant spastic paraplegia type 8 | | | | 83 | | |
HP:0002062 | HP:0002062 | Morphological abnormality of the pyramidal tract | 0 | WASHC5 CL E G H | 9897 | 28984 | OMIM:603563 | Spastic paraplegia 8, autosomal dominant | | | | 83 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | ABCD1 CL E G H | 215 | 61 | ORPHA:139399 | Adrenomyeloneuropathy | | | | 135 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | ALS2 CL E G H | 57679 | 443 | OMIM:607225 | Spastic paralysis, infantile-onset ascending | . | HP:0003593 - Infantile onset | | 114 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | ATL1 CL E G H | 51062 | 11231 | OMIM:182600 | Spastic paraplegia 3, autosomal dominant | | | | 71 | | |
HP:0002062 | HP:0007363 | Aplasia/Hypoplasia of the pyramidal tract | 1 | ATP1A2 CL E G H | 477 | 800 | OMIM:619602 | FETAL AKINESIA, RESPIRATORY INSUFFICIENCY, MICROCEPHALY, POLYMICROGYRIA, AND DYSMORPHIC FACIES; FARIMPD | | | | 239 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | ATP6 CL E G H | 4508 | 7414 | ORPHA:644 | NARP syndrome | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | ATP6 CL E G H | 4508 | 7414 | OMIM:551500 | Neuropathy, ataxia, and retinitis pigmentosa | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | BAZ1B CL E G H | 9031 | 961 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | BCL7B CL E G H | 9275 | 1005 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | BUD23 CL E G H | 114049 | 16405 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | C9ORF72 CL E G H | 203228 | 28337 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 56 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | CHCHD10 CL E G H | 400916 | 15559 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 11 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | CLIP2 CL E G H | 7461 | 2586 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | CPT1C CL E G H | 126129 | 18540 | ORPHA:444099 | Autosomal dominant spastic paraplegia type 73 | | | | 1 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | DCC CL E G H | 1630 | 2701 | ORPHA:238722 | Familial congenital mirror movements | HP:0040282 - Frequent | | | 36 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | DCTN1 CL E G H | 1639 | 2711 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | | | | 86 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | DEAF1 CL E G H | 10522 | 14677 | ORPHA:819 | Smith-Magenis syndrome | | | | 33 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | DNAJC30 CL E G H | 84277 | 16410 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | DNAL4 CL E G H | 10126 | 2955 | ORPHA:238722 | Familial congenital mirror movements | HP:0040282 - Frequent | | | 2 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | EIF4H CL E G H | 7458 | 12741 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | ELN CL E G H | 2006 | 3327 | ORPHA:904 | Williams syndrome | | | | 172 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | FKBP6 CL E G H | 8468 | 3722 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0007363 | Aplasia/Hypoplasia of the pyramidal tract | 1 | FKTN CL E G H | 2218 | 3622 | OMIM:253800 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 | | | | 184 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | FLII CL E G H | 2314 | 3750 | ORPHA:819 | Smith-Magenis syndrome | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | FUS CL E G H | 2521 | 4010 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 105 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | GALC CL E G H | 2581 | 4115 | ORPHA:206448 | Adult Krabbe disease | HP:0040284 - Very rare | | | 160 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | GTF2I CL E G H | 2969 | 4659 | ORPHA:904 | Williams syndrome | | | | 1 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | GTF2IRD1 CL E G H | 9569 | 4661 | ORPHA:904 | Williams syndrome | | | | 1 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | GTF2IRD2 CL E G H | 84163 | 30775 | ORPHA:904 | Williams syndrome | | | | 1 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | IQSEC2 CL E G H | 23096 | 29059 | ORPHA:819 | Smith-Magenis syndrome | | | | 119 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | KPNA3 CL E G H | 3839 | 6396 | ORPHA:171612 | Autosomal dominant spastic paraplegia type 37 | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | L1CAM CL E G H | 3897 | 6470 | OMIM:307000 | Hydrocephalus due to congenital stenosis of aqueduct of sylvius | | | | 134 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | LIMK1 CL E G H | 3984 | 6613 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | METTL27 CL E G H | 155368 | 19068 | ORPHA:904 | Williams syndrome | | | | 1 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | MLXIPL CL E G H | 51085 | 12744 | ORPHA:904 | Williams syndrome | | | | 1 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | NCF1 CL E G H | 653361 | 7660 | ORPHA:904 | Williams syndrome | | | | 13 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | NEFH CL E G H | 4744 | 7737 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | | | | 24 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | NIPA1 CL E G H | 123606 | 17043 | OMIM:600363 | Spastic paraplegia 6, autosomal dominant | | | | 117 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | NTN1 CL E G H | 9423 | 8029 | ORPHA:238722 | Familial congenital mirror movements | HP:0040282 - Frequent | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | PDHB CL E G H | 5162 | 8808 | ORPHA:255138 | Pyruvate dehydrogenase E1-beta deficiency | | | | 37 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | PLP1 CL E G H | 5354 | 9086 | OMIM:312920 | Spastic paraplegia 2, X-linked | | | | 60 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | PRPH CL E G H | 5630 | 9461 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | | | | 25 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | RAD51 CL E G H | 5888 | 9817 | ORPHA:238722 | Familial congenital mirror movements | HP:0040282 - Frequent | | | 9 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | RAI1 CL E G H | 10743 | 9834 | ORPHA:819 | Smith-Magenis syndrome | | | | 150 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | RFC2 CL E G H | 5982 | 9970 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | RTN2 CL E G H | 6253 | 10468 | ORPHA:100993 | Autosomal dominant spastic paraplegia type 12 | | | | 25 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | SLC33A1 CL E G H | 9197 | 95 | ORPHA:171863 | Autosomal dominant spastic paraplegia type 42 | | | | 48 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | SOD1 CL E G H | 6647 | 11179 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | | | | 53 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | SPAST CL E G H | 6683 | 11233 | OMIM:182601 | Spastic paraplegia 4, autosomal dominant | | | | 208 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | SPG11 CL E G H | 80208 | 11226 | OMIM:604360 | Spastic paraplegia 11, autosomal recessive | | | | 287 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | SPG7 CL E G H | 6687 | 11237 | OMIM:607259 | Spastic paraplegia 7, autosomal recessive | | | | 171 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | SQSTM1 CL E G H | 8878 | 11280 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 62 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | STX1A CL E G H | 6804 | 11433 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | TARDBP CL E G H | 23435 | 11571 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 65 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | TBK1 CL E G H | 29110 | 11584 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 20 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | TBL2 CL E G H | 26608 | 11586 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | TMEM270 CL E G H | 135886 | 23018 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | UBAP1 CL E G H | 51271 | 12461 | ORPHA:100993 | Autosomal dominant spastic paraplegia type 12 | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | VCP CL E G H | 7415 | 12666 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 63 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | VPS37D CL E G H | 155382 | 18287 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | WASHC5 CL E G H | 9897 | 28984 | ORPHA:100989 | Autosomal dominant spastic paraplegia type 8 | | | | 83 | | |
HP:0002062 | HP:0002492 | Morphological abnormality of the corticospinal tract | 1 | WASHC5 CL E G H | 9897 | 28984 | OMIM:603563 | Spastic paraplegia 8, autosomal dominant | | | | 83 | | |
HP:0002062 | HP:0100322 | Aplasia of the pyramidal tract | 2 | CL E G H | | | | | | | | | | |
HP:0002062 | HP:0008361 | Corticospinal tract pallor | 2 | CL E G H | | | | | | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | ABCD1 CL E G H | 215 | 61 | ORPHA:139399 | Adrenomyeloneuropathy | HP:0040282 - Frequent | | | 135 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | ATL1 CL E G H | 51062 | 11231 | OMIM:182600 | Spastic paraplegia 3, autosomal dominant | | | | 71 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | ATP6 CL E G H | 4508 | 7414 | ORPHA:644 | NARP syndrome | | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | ATP6 CL E G H | 4508 | 7414 | OMIM:551500 | Neuropathy, ataxia, and retinitis pigmentosa | | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | BAZ1B CL E G H | 9031 | 961 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | BCL7B CL E G H | 9275 | 1005 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | BUD23 CL E G H | 114049 | 16405 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | C9ORF72 CL E G H | 203228 | 28337 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 56 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | CHCHD10 CL E G H | 400916 | 15559 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 11 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | CLIP2 CL E G H | 7461 | 2586 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | CPT1C CL E G H | 126129 | 18540 | ORPHA:444099 | Autosomal dominant spastic paraplegia type 73 | | | | 1 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | DCTN1 CL E G H | 1639 | 2711 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | | | | 86 | | |
HP:0002062 | HP:0007365 | Aplasia/Hypoplasia involving the corticospinal tracts | 2 | DEAF1 CL E G H | 10522 | 14677 | ORPHA:819 | Smith-Magenis syndrome | | | | 33 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | DNAJC30 CL E G H | 84277 | 16410 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | EIF4H CL E G H | 7458 | 12741 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | ELN CL E G H | 2006 | 3327 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 172 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | FKBP6 CL E G H | 8468 | 3722 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0002062 | HP:0007348 | Hypoplasia of the pyramidal tract | 2 | FKTN CL E G H | 2218 | 3622 | OMIM:253800 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 | . | | | 184 | | |
HP:0002062 | HP:0007365 | Aplasia/Hypoplasia involving the corticospinal tracts | 2 | FLII CL E G H | 2314 | 3750 | ORPHA:819 | Smith-Magenis syndrome | | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | FUS CL E G H | 2521 | 4010 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 105 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | GTF2I CL E G H | 2969 | 4659 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | GTF2IRD1 CL E G H | 9569 | 4661 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | GTF2IRD2 CL E G H | 84163 | 30775 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0002062 | HP:0007365 | Aplasia/Hypoplasia involving the corticospinal tracts | 2 | IQSEC2 CL E G H | 23096 | 29059 | ORPHA:819 | Smith-Magenis syndrome | | | | 119 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | KPNA3 CL E G H | 3839 | 6396 | ORPHA:171612 | Autosomal dominant spastic paraplegia type 37 | | | | | | |
HP:0002062 | HP:0007365 | Aplasia/Hypoplasia involving the corticospinal tracts | 2 | L1CAM CL E G H | 3897 | 6470 | OMIM:307000 | Hydrocephalus due to congenital stenosis of aqueduct of sylvius | | | | 134 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | LIMK1 CL E G H | 3984 | 6613 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | METTL27 CL E G H | 155368 | 19068 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | MLXIPL CL E G H | 51085 | 12744 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | NCF1 CL E G H | 653361 | 7660 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 13 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | NEFH CL E G H | 4744 | 7737 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | | | | 24 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | NIPA1 CL E G H | 123606 | 17043 | OMIM:600363 | Spastic paraplegia 6, autosomal dominant | | | | 117 | | |
HP:0002062 | HP:0007365 | Aplasia/Hypoplasia involving the corticospinal tracts | 2 | PDHB CL E G H | 5162 | 8808 | ORPHA:255138 | Pyruvate dehydrogenase E1-beta deficiency | | | | 37 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | PLP1 CL E G H | 5354 | 9086 | OMIM:312920 | Spastic paraplegia 2, X-linked | | | | 60 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | PRPH CL E G H | 5630 | 9461 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | | | | 25 | | |
HP:0002062 | HP:0007365 | Aplasia/Hypoplasia involving the corticospinal tracts | 2 | RAI1 CL E G H | 10743 | 9834 | ORPHA:819 | Smith-Magenis syndrome | | | | 150 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | RFC2 CL E G H | 5982 | 9970 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | RTN2 CL E G H | 6253 | 10468 | ORPHA:100993 | Autosomal dominant spastic paraplegia type 12 | | | | 25 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | SLC33A1 CL E G H | 9197 | 95 | ORPHA:171863 | Autosomal dominant spastic paraplegia type 42 | | | | 48 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | SOD1 CL E G H | 6647 | 11179 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | | | | 53 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | SPAST CL E G H | 6683 | 11233 | OMIM:182601 | Spastic paraplegia 4, autosomal dominant | | | | 208 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | SPG11 CL E G H | 80208 | 11226 | OMIM:604360 | Spastic paraplegia 11, autosomal recessive | | | | 287 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | SPG7 CL E G H | 6687 | 11237 | OMIM:607259 | Spastic paraplegia 7, autosomal recessive | | | | 171 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | SQSTM1 CL E G H | 8878 | 11280 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 62 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | STX1A CL E G H | 6804 | 11433 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | TARDBP CL E G H | 23435 | 11571 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 65 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | TBK1 CL E G H | 29110 | 11584 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 20 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | TBL2 CL E G H | 26608 | 11586 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | TMEM270 CL E G H | 135886 | 23018 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | UBAP1 CL E G H | 51271 | 12461 | ORPHA:100993 | Autosomal dominant spastic paraplegia type 12 | | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | VCP CL E G H | 7415 | 12666 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | | | | 63 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | VPS37D CL E G H | 155382 | 18287 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | WASHC5 CL E G H | 9897 | 28984 | ORPHA:100989 | Autosomal dominant spastic paraplegia type 8 | | | | 83 | | |
HP:0002062 | HP:0007372 | Atrophy/Degeneration involving the corticospinal tracts | 2 | WASHC5 CL E G H | 9897 | 28984 | OMIM:603563 | Spastic paraplegia 8, autosomal dominant | | | | 83 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | ATL1 CL E G H | 51062 | 11231 | OMIM:182600 | Spastic paraplegia 3, autosomal dominant | . | | | 71 | | |
HP:0002062 | HP:0007117 | Corticospinal tract atrophy | 3 | ATP6 CL E G H | 4508 | 7414 | ORPHA:644 | NARP syndrome | HP:0040282 - Frequent | | | | | |
HP:0002062 | HP:0007117 | Corticospinal tract atrophy | 3 | ATP6 CL E G H | 4508 | 7414 | OMIM:551500 | Neuropathy, ataxia, and retinitis pigmentosa | . | | | | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | C9ORF72 CL E G H | 203228 | 28337 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | HP:0040282 - Frequent | | | 56 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | CHCHD10 CL E G H | 400916 | 15559 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | HP:0040282 - Frequent | | | 11 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | CPT1C CL E G H | 126129 | 18540 | ORPHA:444099 | Autosomal dominant spastic paraplegia type 73 | HP:0040281 - Very frequent | | | 1 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | DCTN1 CL E G H | 1639 | 2711 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | . | | | 86 | | |
HP:0002062 | HP:0007016 | Corticospinal tract hypoplasia | 3 | DEAF1 CL E G H | 10522 | 14677 | ORPHA:819 | Smith-Magenis syndrome | HP:0040281 - Very frequent | | | 33 | | |
HP:0002062 | HP:0007016 | Corticospinal tract hypoplasia | 3 | FLII CL E G H | 2314 | 3750 | ORPHA:819 | Smith-Magenis syndrome | HP:0040281 - Very frequent | | | | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | FUS CL E G H | 2521 | 4010 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | HP:0040282 - Frequent | | | 105 | | |
HP:0002062 | HP:0007016 | Corticospinal tract hypoplasia | 3 | IQSEC2 CL E G H | 23096 | 29059 | ORPHA:819 | Smith-Magenis syndrome | HP:0040281 - Very frequent | | | 119 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | KPNA3 CL E G H | 3839 | 6396 | ORPHA:171612 | Autosomal dominant spastic paraplegia type 37 | HP:0040281 - Very frequent | | | | | |
HP:0002062 | HP:0007016 | Corticospinal tract hypoplasia | 3 | L1CAM CL E G H | 3897 | 6470 | OMIM:307000 | Hydrocephalus due to congenital stenosis of aqueduct of sylvius | . | | | 134 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | NEFH CL E G H | 4744 | 7737 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | . | | | 24 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | NIPA1 CL E G H | 123606 | 17043 | OMIM:600363 | Spastic paraplegia 6, autosomal dominant | . | | | 117 | | |
HP:0002062 | HP:0007016 | Corticospinal tract hypoplasia | 3 | PDHB CL E G H | 5162 | 8808 | ORPHA:255138 | Pyruvate dehydrogenase E1-beta deficiency | HP:0040283 - Occasional | | | 37 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | PLP1 CL E G H | 5354 | 9086 | OMIM:312920 | Spastic paraplegia 2, X-linked | . | | | 60 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | PRPH CL E G H | 5630 | 9461 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | . | | | 25 | | |
HP:0002062 | HP:0007016 | Corticospinal tract hypoplasia | 3 | RAI1 CL E G H | 10743 | 9834 | ORPHA:819 | Smith-Magenis syndrome | HP:0040281 - Very frequent | | | 150 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | RTN2 CL E G H | 6253 | 10468 | ORPHA:100993 | Autosomal dominant spastic paraplegia type 12 | HP:0040281 - Very frequent | | | 25 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | SLC33A1 CL E G H | 9197 | 95 | ORPHA:171863 | Autosomal dominant spastic paraplegia type 42 | HP:0040281 - Very frequent | | | 48 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | SOD1 CL E G H | 6647 | 11179 | OMIM:105400 | Amyotrophic lateral sclerosis 1 | . | | | 53 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | SPAST CL E G H | 6683 | 11233 | OMIM:182601 | Spastic paraplegia 4, autosomal dominant | . | | | 208 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | SPG11 CL E G H | 80208 | 11226 | OMIM:604360 | Spastic paraplegia 11, autosomal recessive | . | | | 287 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | SPG7 CL E G H | 6687 | 11237 | OMIM:607259 | Spastic paraplegia 7, autosomal recessive | . | | | 171 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | SQSTM1 CL E G H | 8878 | 11280 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | HP:0040282 - Frequent | | | 62 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | TARDBP CL E G H | 23435 | 11571 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | HP:0040282 - Frequent | | | 65 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | TBK1 CL E G H | 29110 | 11584 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | HP:0040282 - Frequent | | | 20 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | UBAP1 CL E G H | 51271 | 12461 | ORPHA:100993 | Autosomal dominant spastic paraplegia type 12 | HP:0040281 - Very frequent | | | | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | VCP CL E G H | 7415 | 12666 | ORPHA:275872 | Frontotemporal dementia with motor neuron disease | HP:0040282 - Frequent | | | 63 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | WASHC5 CL E G H | 9897 | 28984 | ORPHA:100989 | Autosomal dominant spastic paraplegia type 8 | HP:0040281 - Very frequent | | | 83 | | |
HP:0002062 | HP:0002314 | Degeneration of the lateral corticospinal tracts | 3 | WASHC5 CL E G H | 9897 | 28984 | OMIM:603563 | Spastic paraplegia 8, autosomal dominant | . | | | 83 | | |