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	paraplegia

Disease ID	884
Disease	paraplegia
Definition	Severe or complete loss of motor function in the lower extremities and lower portions of the trunk. This condition is most often associated with SPINAL CORD DISEASES, although BRAIN DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; NEUROMUSCULAR DISEASES; and MUSCULAR DISEASES may also cause bilateral leg weakness.
Synonym	extremities lower paralysis extremity paralysis, lower leg paralysis lower paraplegia paralysis of both lower limbs paralysis, legs paralysis, lower extremities paralysis, lower limbs paraplegia (complete or partial paralysis of legs) paraplegia (disorder) paraplegia [disease/finding] paraplegia nos paraplegia, lower paraplegias
DOID	DOID:607
UMLS	C0030486
MeSH	D010264
SNOMED-CT	SNOMEDCT_US_2016_09_01:60389000
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:46) C0022116 \| ischemia \| 6 C0004134 \| ataxia \| 4 C0007758 \| cerebellar ataxia \| 4 C0442874 \| neuropathy \| 4 C0270921 \| axonal neuropathy \| 3 C0029124 \| optic atrophy \| 3 C0026975 \| myelitis \| 2 C0031117 \| peripheral neuropathy \| 2 C0025362 \| mental retardation \| 2 C0039730 \| thalassemia \| 2 C0003486 \| aortic aneurysm \| 2 C0011127 \| pressure sores \| 2 C0018099 \| gout \| 1 C0011649 \| dermoid cyst \| 1 C0031485 \| phenylketonuria \| 1 C0086543 \| cataracts \| 1 C0001080 \| achondroplasia \| 1 C0027873 \| neuromyelitis optica \| 1 C0162871 \| abdominal aortic aneurysm \| 1 C0030486 \| paraplegia \| 1 C0022116 \| ischaemia \| 1 C0007222 \| cardiovascular disease \| 1 C0221069 \| anterior spinal artery syndrome \| 1 C0004943 \| behcet's disease \| 1 C0042373 \| vascular disease \| 1 C0007760 \| cerebellar dysfunction \| 1 C0022821 \| kyphosis \| 1 C0151313 \| sensory neuropathy \| 1 C0028738 \| nystagmus \| 1 C0017919 \| glycogen storage disease \| 1 C0497327 \| dementia \| 1 C0005283 \| beta thalassemia \| 1 C0812437 \| oculodentodigital dysplasia \| 1 C0018916 \| hemangioma \| 1 C0029438 \| gorham's disease \| 1 C0035078 \| renal failure \| 1 C0038012 \| spondylitis \| 1 C0024236 \| lymphoedema \| 1 C0029132 \| optic neuropathy \| 1 C0037944 \| spinal stenosis \| 1 C0037928 \| myelopathy \| 1 C0019937 \| horner's syndrome \| 1 C0041296 \| tuberculosis \| 1 C0013502 \| hydatid cyst \| 1 C0206754 \| neuroendocrine tumor \| 1 C0024623 \| gastric cancer \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:56) 3329 \| HSPD1 \| UniProtKB-KW 26580 \| BSCL2 \| UniProtKB-KW 10667 \| FARS2 \| UniProtKB-KW 57498 \| KIDINS220 \| UniProtKB-KW 7345 \| UCHL1 \| UniProtKB-KW 83636 \| C19orf12 \| UniProtKB-KW 6683 \| SPAST \| UniProtKB-KW 3897 \| L1CAM \| UniProtKB-KW;GHR 80208 \| SPG11 \| UniProtKB-KW 9895 \| TECPR2 \| UniProtKB-KW 10717 \| AP4B1 \| UniProtKB-KW 6687 \| SPG7 \| CTD_human;UniProtKB-KW 126129 \| CPT1C \| UniProtKB-KW 23431 \| AP4E1 \| UniProtKB-KW 9197 \| SLC33A1 \| UniProtKB-KW 123606 \| NIPA1 \| UniProtKB-KW 57531 \| HACE1 \| UniProtKB-KW 22978 \| NT5C2 \| UniProtKB-KW 11154 \| AP4S1 \| UniProtKB-KW 547 \| KIF1A \| UniProtKB-KW 4099 \| MAG \| UniProtKB-KW 23400 \| ATP13A2 \| UniProtKB-KW 823 \| CAPN1 \| UniProtKB-KW 10613 \| ERLIN1 \| UniProtKB-KW 10908 \| PNPLA6 \| UniProtKB-KW 51062 \| ATL1 \| UniProtKB-KW 271 \| AMPD2 \| UniProtKB-KW 9907 \| AP5Z1 \| UniProtKB-KW 51324 \| SPG21 \| UniProtKB-KW 23111 \| SPG20 \| UniProtKB-KW;GHR 5354 \| PLP1 \| UniProtKB-KW 5832 \| ALDH18A1 \| UniProtKB-KW 79152 \| FA2H \| UniProtKB-KW 80821 \| DDHD1 \| UniProtKB-KW 23259 \| DDHD2 \| UniProtKB-KW 137492 \| VPS37A \| UniProtKB-KW 23204 \| ARL6IP1 \| UniProtKB-KW 2583 \| B4GALNT1 \| UniProtKB-KW 118813 \| ZFYVE27 \| UniProtKB-KW 11160 \| ERLIN2 \| UniProtKB-KW 91574 \| C12orf65 \| UniProtKB-KW 9420 \| CYP7B1 \| UniProtKB-KW 3798 \| KIF5A \| UniProtKB-KW 953 \| ENTPD1 \| UniProtKB-KW 10342 \| TFG \| UniProtKB-KW 9179 \| AP4M1 \| UniProtKB-KW 113612 \| CYP2U1 \| UniProtKB-KW 57165 \| GJC2 \| UniProtKB-KW 51308 \| REEP2 \| UniProtKB-KW 65055 \| REEP1 \| UniProtKB-KW 200205 \| IBA57 \| UniProtKB-KW 23503 \| ZFYVE26 \| UniProtKB-KW 6253 \| RTN2 \| UniProtKB-KW 64837 \| KLC2 \| UniProtKB-KW 57704 \| GBA2 \| UniProtKB-KW 25778 \| DSTYK \| UniProtKB-KW
Inferring Gene	Entrez_id \| Symbol \| Resource(Total Genes:2) 9197 \| SLC33A1 \| CIPHER 6687 \| SPG7 \| CTD_human
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:249) 26090 \| ABHD12 \| 2.19 \| DISEASES 10121 \| ACTR1A \| 2.196 \| DISEASES 2334 \| AFF2 \| 1.137 \| DISEASES 10555 \| AGPAT2 \| 3.315 \| DISEASES 199 \| AIF1 \| 1.296 \| DISEASES 64400 \| AKTIP \| 1.083 \| DISEASES 5832 \| ALDH18A1 \| 2.767 \| DISEASES 224 \| ALDH3A2 \| 2.368 \| DISEASES 279 \| AMY2A \| 1.18 \| DISEASES 1174 \| AP1S1 \| 1.632 \| DISEASES 9179 \| AP4M1 \| 2.834 \| DISEASES 91056 \| AP5B1 \| 3.261 \| DISEASES 54840 \| APTX \| 1.371 \| DISEASES 361 \| AQP4 \| 2.468 \| DISEASES 393 \| ARHGAP4 \| 1.403 \| DISEASES 55210 \| ATAD3A \| 1.743 \| DISEASES 51062 \| ATL1 \| 6.933 \| DISEASES 64225 \| ATL2 \| 2.352 \| DISEASES 25923 \| ATL3 \| 3.218 \| DISEASES 23400 \| ATP13A2 \| 2.255 \| DISEASES 493 \| ATP2B4 \| 1.925 \| DISEASES 6311 \| ATXN2 \| 1.045 \| DISEASES 4287 \| ATXN3 \| 2.945 \| DISEASES 6314 \| ATXN7 \| 2.443 \| DISEASES 26053 \| AUTS2 \| 1.07 \| DISEASES 2583 \| B4GALNT1 \| 3.271 \| DISEASES 617 \| BCS1L \| 1.779 \| DISEASES 23299 \| BICD2 \| 3.994 \| DISEASES 655 \| BMP7 \| 2.369 \| DISEASES 659 \| BMPR2 \| 1.042 \| DISEASES 388962 \| BOLA3 \| 1.666 \| DISEASES 26580 \| BSCL2 \| 4.749 \| DISEASES 84529 \| C15orf41 \| 2.878 \| DISEASES 400359 \| C15orf53 \| 2.608 \| DISEASES 83636 \| C19orf12 \| 2.005 \| DISEASES 203228 \| C9orf72 \| 1.581 \| DISEASES 773 \| CACNA1A \| 1.585 \| DISEASES 785 \| CACNB4 \| 1.193 \| DISEASES 796 \| CALCA \| 2.03 \| DISEASES 152137 \| CCDC50 \| 1.915 \| DISEASES 9973 \| CCS \| 1.191 \| DISEASES 10575 \| CCT4 \| 1.32 \| DISEASES 8556 \| CDC14A \| 1.43 \| DISEASES 1003 \| CDH5 \| 2.951 \| DISEASES 1028 \| CDKN1C \| 2.939 \| DISEASES 10390 \| CEPT1 \| 1.94 \| DISEASES 55636 \| CHD7 \| 1.414 \| DISEASES 57680 \| CHD8 \| 1.068 \| DISEASES 5119 \| CHMP1A \| 1.959 \| DISEASES 57132 \| CHMP1B \| 2.536 \| DISEASES 10970 \| CKAP4 \| 1.467 \| DISEASES 1267 \| CNP \| 1.759 \| DISEASES 54875 \| CNTLN \| 1.433 \| DISEASES 27255 \| CNTN6 \| 1.505 \| DISEASES 51287 \| COA4 \| 1.933 \| DISEASES 53844 \| COPG2IT1 \| 2.916 \| DISEASES 84701 \| COX4I2 \| 1.047 \| DISEASES 1485 \| CTAG1B \| 1.82 \| DISEASES 1490 \| CTGF \| 2.531 \| DISEASES 1496 \| CTNNA2 \| 1.139 \| DISEASES 1499 \| CTNNB1 \| 1.229 \| DISEASES 2919 \| CXCL1 \| 2.356 \| DISEASES 6387 \| CXCL12 \| 1.384 \| DISEASES 113612 \| CYP2U1 \| 4.757 \| DISEASES 80067 \| DCAF17 \| 1.101 \| DISEASES 1639 \| DCTN1 \| 2.874 \| DISEASES 80821 \| DDHD1 \| 4.661 \| DISEASES 23259 \| DDHD2 \| 4.916 \| DISEASES 1741 \| DLG3 \| 1.665 \| DISEASES 3300 \| DNAJB2 \| 2.505 \| DISEASES 1785 \| DNM2 \| 1.65 \| DISEASES 1786 \| DNMT1 \| 1.024 \| DISEASES 1825 \| DSC3 \| 1.204 \| DISEASES 79075 \| DSCC1 \| 2.171 \| DISEASES 25778 \| DSTYK \| 2.582 \| DISEASES 1778 \| DYNC1H1 \| 3.869 \| DISEASES 1781 \| DYNC1I2 \| 1.495 \| DISEASES 54583 \| EGLN1 \| 1.613 \| DISEASES 2060 \| EPS15 \| 1.889 \| DISEASES 2117 \| ETV3 \| 1.332 \| DISEASES 51010 \| EXOSC3 \| 2.62 \| DISEASES 51571 \| FAM49B \| 1.64 \| DISEASES 283742 \| FAM98B \| 2.75 \| DISEASES 22862 \| FNDC3A \| 1.738 \| DISEASES 2395 \| FXN \| 1.876 \| DISEASES 57704 \| GBA2 \| 4.34 \| DISEASES 57733 \| GBA3 \| 1.639 \| DISEASES 2632 \| GBE1 \| 1.249 \| DISEASES 2635 \| GBP3 \| 2.059 \| DISEASES 2643 \| GCH1 \| 2.605 \| DISEASES 2687 \| GGT5 \| 1.413 \| DISEASES 2705 \| GJB1 \| 2.095 \| DISEASES 57165 \| GJC2 \| 4.284 \| DISEASES 349149 \| GJC3 \| 1.536 \| DISEASES 51218 \| GLRX5 \| 1.212 \| DISEASES 149775 \| GNAS-AS1 \| 2.169 \| DISEASES 10243 \| GPHN \| 1.527 \| DISEASES 2887 \| GRB10 \| 2.834 \| DISEASES 3039 \| HBA1 \| 2.878 \| DISEASES 3142 \| HLX \| 1.104 \| DISEASES 3178 \| HNRNPA1 \| 1.661 \| DISEASES 3198 \| HOXA1 \| 1.046 \| DISEASES 3329 \| HSPD1 \| 2.447 \| DISEASES 200205 \| IBA57 \| 1.762 \| DISEASES 3481 \| IGF2 \| 2.494 \| DISEASES 3482 \| IGF2R \| 2.129 \| DISEASES 10989 \| IMMT \| 1.33 \| DISEASES 134728 \| IRAK1BP1 \| 2.049 \| DISEASES 9798 \| IST1 \| 3.552 \| DISEASES 83737 \| ITCH \| 3.043 \| DISEASES 3713 \| IVL \| 1.348 \| DISEASES 56704 \| JPH1 \| 2.155 \| DISEASES 102723508 \| KANTR \| 3.208 \| DISEASES 11104 \| KATNA1 \| 3.726 \| DISEASES 10300 \| KATNB1 \| 2.008 \| DISEASES 3748 \| KCNC3 \| 1.037 \| DISEASES 10984 \| KCNQ1OT1 \| 2.625 \| DISEASES 23303 \| KIF13B \| 2.84 \| DISEASES 547 \| KIF1A \| 4.455 \| DISEASES 10749 \| KIF1C \| 3.473 \| DISEASES 3798 \| KIF5A \| 5.538 \| DISEASES 3800 \| KIF5C \| 3.175 \| DISEASES 147700 \| KLC3 \| 2.074 \| DISEASES 9314 \| KLF4 \| 1.667 \| DISEASES 11202 \| KLK8 \| 1.622 \| DISEASES 3895 \| KTN1 \| 1.281 \| DISEASES 3897 \| L1CAM \| 5.054 \| DISEASES 3916 \| LAMP1 \| 1.084 \| DISEASES 8861 \| LDB1 \| 2.98 \| DISEASES 1130 \| LYST \| 2.193 \| DISEASES 4099 \| MAG \| 1.52 \| DISEASES 4133 \| MAP2 \| 2.153 \| DISEASES 4155 \| MBP \| 2.97 \| DISEASES 55384 \| MEG3 \| 2.197 \| DISEASES 4212 \| MEIS2 \| 1.228 \| DISEASES 317751 \| MESTIT1 \| 2.951 \| DISEASES 4326 \| MMP17 \| 1.206 \| DISEASES 4318 \| MMP9 \| 1.382 \| DISEASES 84545 \| MRPL43 \| 2.507 \| DISEASES 22921 \| MSRB2 \| 1.428 \| DISEASES 4535 \| MT-ND1 \| 1.919 \| DISEASES 4580 \| MTX1 \| 1.077 \| DISEASES 283446 \| MYO1H \| 2.934 \| DISEASES 25915 \| NDUFAF3 \| 1.407 \| DISEASES 4734 \| NEDD4 \| 1.234 \| DISEASES 27247 \| NFU1 \| 1.372 \| DISEASES 123606 \| NIPA1 \| 5.676 \| DISEASES 57185 \| NIPAL3 \| 2.916 \| DISEASES 10528 \| NOP56 \| 2.297 \| DISEASES 27035 \| NOX1 \| 1.34 \| DISEASES 4868 \| NPHS1 \| 1.16 \| DISEASES 7827 \| NPHS2 \| 1.796 \| DISEASES 4897 \| NRCAM \| 3.82 \| DISEASES 4958 \| OMD \| 1.404 \| DISEASES 4976 \| OPA1 \| 1.895 \| DISEASES 5071 \| PARK2 \| 1.166 \| DISEASES 55486 \| PARL \| 1.352 \| DISEASES 23089 \| PEG10 \| 1.843 \| DISEASES 5178 \| PEG3 \| 1.644 \| DISEASES 192111 \| PGAM5 \| 1.766 \| DISEASES 55361 \| PI4K2A \| 1.189 \| DISEASES 8605 \| PLA2G4C \| 1.596 \| DISEASES 8398 \| PLA2G6 \| 2.033 \| DISEASES 5325 \| PLAGL1 \| 1.94 \| DISEASES 285848 \| PNPLA1 \| 1.51 \| DISEASES 10908 \| PNPLA6 \| 4.518 \| DISEASES 375775 \| PNPLA7 \| 2.626 \| DISEASES 11128 \| POLR3A \| 1.519 \| DISEASES 10631 \| POSTN \| 1.082 \| DISEASES 8541 \| PPFIA3 \| 1.775 \| DISEASES 5663 \| PSEN1 \| 1.518 \| DISEASES 9791 \| PTDSS1 \| 1.617 \| DISEASES 5788 \| PTPRC \| 2.227 \| DISEASES 8437 \| RASAL1 \| 2.007 \| DISEASES 1104 \| RCC1 \| 1.624 \| DISEASES 65055 \| REEP1 \| 6.084 \| DISEASES 7905 \| REEP5 \| 2.399 \| DISEASES 55188 \| RIC8B \| 1.806 \| DISEASES 79621 \| RNASEH2B \| 2.367 \| DISEASES 6049 \| RNF6 \| 2.173 \| DISEASES 6093 \| ROCK1 \| 1.298 \| DISEASES 6164 \| RPL34 \| 3.153 \| DISEASES 6195 \| RPS6KA1 \| 1.345 \| DISEASES 26750 \| RPS6KC1 \| 2.599 \| DISEASES 3921 \| RPSA \| 1.459 \| DISEASES 388015 \| RTL1 \| 2.169 \| DISEASES 10313 \| RTN3 \| 2.145 \| DISEASES 6275 \| S100A4 \| 6.09 \| DISEASES 26278 \| SACS \| 3.504 \| DISEASES 9919 \| SEC16A \| 1.92 \| DISEASES 80031 \| SEMA6D \| 1.608 \| DISEASES 84947 \| SERAC1 \| 1.054 \| DISEASES 462 \| SERPINC1 \| 1.484 \| DISEASES 871 \| SERPINH1 \| 1.712 \| DISEASES 9990 \| SLC12A6 \| 3.148 \| DISEASES 123041 \| SLC24A4 \| 1.309 \| DISEASES 10166 \| SLC25A15 \| 2.19 \| DISEASES 55676 \| SLC30A6 \| 2.515 \| DISEASES 9197 \| SLC33A1 \| 4.662 \| DISEASES 91252 \| SLC39A13 \| 1.736 \| DISEASES 9152 \| SLC6A5 \| 1.006 \| DISEASES 6547 \| SLC8A3 \| 1.048 \| DISEASES 4088 \| SMAD3 \| 2.451 \| DISEASES 4090 \| SMAD5 \| 2.087 \| DISEASES 26801 \| SNORD48 \| 1.199 \| DISEASES 6641 \| SNTB1 \| 1.908 \| DISEASES 29907 \| SNX15 \| 3.413 \| DISEASES 80320 \| SP6 \| 1.811 \| DISEASES 6683 \| SPAST \| 7.678 \| DISEASES 23111 \| SPG20 \| 5.732 \| DISEASES 6709 \| SPTAN1 \| 1.83 \| DISEASES 8878 \| SQSTM1 \| 1.439 \| DISEASES 27286 \| SRPX2 \| 1.138 \| DISEASES 6483 \| ST3GAL2 \| 1.44 \| DISEASES 8869 \| ST3GAL5 \| 1.288 \| DISEASES 29906 \| ST8SIA5 \| 3.16 \| DISEASES 6836 \| SURF4 \| 2.322 \| DISEASES 11346 \| SYNPO \| 1.662 \| DISEASES 7062 \| TCHH \| 1.065 \| DISEASES 9895 \| TECPR2 \| 4.549 \| DISEASES 7042 \| TGFB2 \| 1.158 \| DISEASES 7048 \| TGFBR2 \| 1.088 \| DISEASES 1678 \| TIMM8A \| 1.427 \| DISEASES 145942 \| TMCO5A \| 2.863 \| DISEASES 83857 \| TMTC1 \| 2.962 \| DISEASES 7124 \| TNF \| 1.002 \| DISEASES 3842 \| TNPO1 \| 1.237 \| DISEASES 22906 \| TRAK1 \| 2.501 \| DISEASES 66008 \| TRAK2 \| 2.085 \| DISEASES 23321 \| TRIM2 \| 1.776 \| DISEASES 57113 \| TRPC7 \| 1.185 \| DISEASES 25987 \| TSKU \| 1.273 \| DISEASES 10100 \| TSPAN2 \| 1.481 \| DISEASES 7106 \| TSPAN4 \| 2.269 \| DISEASES 284076 \| TTLL6 \| 2.424 \| DISEASES 23025 \| UNC13A \| 1.175 \| DISEASES 10497 \| UNC13B \| 1.168 \| DISEASES 285175 \| UNC80 \| 1.862 \| DISEASES 57558 \| USP35 \| 2.575 \| DISEASES 6843 \| VAMP1 \| 1.31 \| DISEASES 7415 \| VCP \| 2.444 \| DISEASES 79674 \| VEPH1 \| 2.119 \| DISEASES 51699 \| VPS29 \| 2.494 \| DISEASES 7454 \| WAS \| 1.064 \| DISEASES 653440 \| WASH6P \| 3.19 \| DISEASES 11152 \| WDR45 \| 2.056 \| DISEASES 55432 \| YOD1 \| 1.439 \| DISEASES 51530 \| ZC3HC1 \| 1.441 \| DISEASES 118813 \| ZFYVE27 \| 4.895 \| DISEASES
Locus	(Waiting for update.)

Disease ID	884
Disease	paraplegia
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:71) HP:0002079 \| Hypoplasia of the corpus callosum \| 18 HP:0001249 \| Mental retardation \| 7 HP:0012531 \| Pain \| 6 HP:0003690 \| Limb weakness \| 6 HP:0001251 \| Ataxia \| 5 HP:0003477 \| Peripheral axonal neuropathy \| 4 HP:0100310 \| Extradural hematoma \| 3 HP:0012486 \| Inflammation of spinal cord \| 3 HP:0001284 \| Areflexia \| 3 HP:0000648 \| Optic-nerve degeneration \| 3 HP:0001337 \| Tremor \| 2 HP:0002176 \| Spinal cord compression \| 2 HP:0012399 \| Bedsore \| 2 HP:0001263 \| Developmental retardation \| 2 HP:0030731 \| Carcinoma \| 2 HP:0004947 \| Arteriovenous fistula \| 2 HP:0003474 \| Sensory impairment \| 2 HP:0001297 \| Cerebral vascular events \| 2 HP:0001288 \| Gait disturbance \| 2 HP:0009830 \| Peripheral neuritis \| 2 HP:0040078 \| Axonal degeneration \| 2 HP:0001257 \| Spasticity \| 2 HP:0001268 \| Mental deterioration \| 2 HP:0004942 \| Aortic aneurysm \| 2 HP:0000519 \| Cataracts, lenticular, bilateral \| 1 HP:0000016 \| Urinary retention \| 1 HP:0100543 \| Cognitive deficits \| 1 HP:0012126 \| Gastric cancer \| 1 HP:0000083 \| Renal insufficiency \| 1 HP:0001028 \| Strawberry mark \| 1 HP:0003390 \| Sensory axonal neuropathy \| 1 HP:0003202 \| Neurogenic muscle atrophy, especially in the lower limbs \| 1 HP:0001548 \| Overgrowth \| 1 HP:0001300 \| Parkinsonism \| 1 HP:0002098 \| Respiratory distress \| 1 HP:0030834 \| Shoulder pain \| 1 HP:0001138 \| Damaged optic nerve \| 1 HP:0002617 \| Aneurysmal dilatation \| 1 HP:0007002 \| Motor axonal neuropathy \| 1 HP:0003401 \| Paresthesia \| 1 HP:0002647 \| Aortic dissection \| 1 HP:0100749 \| Thoracic pain \| 1 HP:0000969 \| Dropsy \| 1 HP:0001945 \| Fever \| 1 HP:0001260 \| Dysarthric speech \| 1 HP:0003487 \| Extensor plantar reflexes \| 1 HP:0002385 \| Paraparesis \| 1 HP:0001004 \| Lymphatic obstruction \| 1 HP:0001252 \| Hypotonia \| 1 HP:0000726 \| Dementia \| 1 HP:0007178 \| Motor polyneuropathy \| 1 HP:0003470 \| Inability to move \| 1 HP:0100561 \| Spinal cord lesion \| 1 HP:0200040 \| Epidermal inclusion cyst \| 1 HP:0010550 \| Paraplegia \| 1 HP:0001997 \| Gout \| 1 HP:0000020 \| Bladder incontinence \| 1 HP:0002196 \| Myelopathy \| 1 HP:0002607 \| Anal incontinence \| 1 HP:0002839 \| Urinary bladder sphincter dysfunction \| 1 HP:0000708 \| Behavioral problems \| 1 HP:0002808 \| Gibbus deformity \| 1 HP:0002277 \| Horner's syndrome \| 1 HP:0009058 \| Muscle lipidosis \| 1 HP:0000763 \| Sensory neuropathy \| 1 HP:0003416 \| Spinal canal stenosis \| 1 HP:0004953 \| Abdominal aortic aneurysm \| 1 HP:0005881 \| Spinal instability \| 1 HP:0000518 \| Cataract \| 1 HP:0100242 \| Sarcoma \| 1 HP:0000639 \| Nystagmus \| 1

Disease ID	884
Disease	paraplegia
Manually Symptom	UMLS \| Name(Total Manually Symptoms:66) C2707258 \| infections C2678504 \| osteoporosis C2598155 \| pain C1963244 \| supraventricular tachycardia C1963087 \| constipation C1961100 \| erectile dysfunction C1546602 \| diverticulum C1540912 \| hypereosinophilic syndrome C1258215 \| ileus C1000483 \| anemia C0700208 \| scoliosis C0699885 \| bladder cancer C0694550 \| recurrent pneumonia C0600139 \| carcinoma of the prostate C0575081 \| gait disturbance C0494752 \| diaphragmatic hernia C0452221 \| vertebral osteomyelitis C0451641 \| urolithiasis C0426768 \| o sign C0423716 \| neuropathic pain C0401149 \| chronic constipation C0392525 \| nephrolithiasis C0271708 \| fasting hypoglycemia C0270777 \| spinal cord edema C0263661 \| osteoarthropathies C0235031 \| neurologic symptoms C0221166 \| paraparesis C0152256 \| disuse osteoporosis C0085697 \| chronic pyelonephritis C0042580 \| vesicoureteral reflux C0042580 \| vesico-ureteric reflux C0042580 \| vesico-ureteral reflux C0042075 \| urinary tract disorders C0042029 \| urinary infection C0039070 \| syncope C0038828 \| superior mesenteric artery syndrome C0038525 \| subarachnoid hemorrhage C0037763 \| spasms C0037315 \| sleep apnoea C0037299 \| skin ulceration C0034216 \| pyonephrosis C0034186 \| pyelonephritis C0034065 \| pulmonary embolism C0033117 \| priapism C0030925 \| perforated peptic ulcer C0030920 \| peptic ulcer C0029440 \| osteoma C0027122 \| myositis ossificans C0026838 \| spasticity C0026826 \| hypertonia C0022661 \| end-stage renal disease C0022661 \| chronic renal failure C0022408 \| arthropathies C0020903 \| illusions C0020440 \| hypercapnia C0020295 \| hydronephrosis C0016053 \| fibromyositis C0012616 \| disarticulation C0011127 \| pressure sores C0011127 \| decubitus ulcers C0011127 \| decubitus ulcer C0011127 \| bedsores C0010701 \| cystosarcoma phyllodes C0009024 \| clonus C0002726 \| amyloidosis C0001080 \| chondrodystrophia fetalis
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:6) C0030193 \| pain \| 7 C0011127 \| pressure sores \| 2 C0426768 \| o sign \| 2 C0026838 \| spasticity \| 2 C0575081 \| gait disturbance \| 2 C0221166 \| paraparesis \| 1

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:0)
(Waiting for update.)

GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)

GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)

Mapped by lexical matching(Total Items:0)
(Waiting for update.)

Mapped by homologous gene(Total Items:0)
(Waiting for update.)

Disease ID	884
Disease	paraplegia
Case	(Waiting for update.)

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