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Pediatric Disease Annotations & Medicines



   hemiplegia
  

Disease ID 1129
Disease hemiplegia
Definition
Severe or complete loss of motor function on one side of the body. This condition is usually caused by BRAIN DISEASES that are localized to the cerebral hemisphere opposite to the side of weakness. Less frequently, BRAIN STEM lesions; cervical SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; and other conditions may manifest as hemiplegia. The term hemiparesis (see PARESIS) refers to mild to moderate weakness involving one side of the body.
Synonym
hemiplegia (disorder)
hemiplegia (paralysis on one side)
hemiplegia [disease/finding]
hemiplegia nos
hemiplegia nos (disorder)
hemiplegia, nos
hemiplegia, unspecified
hemiplegias
paralysis of one side of body
paralysis one side of body
DOID
UMLS
C0018991
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:31)
C0007785  |  cerebral infarct  |  8
C0007785  |  cerebral infarction  |  8
C0042373  |  vascular disease  |  3
C0015464  |  facial palsy  |  3
C0007789  |  cerebral palsy  |  3
C0011847  |  diabetes  |  3
C0149931  |  migraine  |  2
C0003537  |  aphasia  |  2
C0020538  |  hypertension  |  2
C0015464  |  facial nerve palsy  |  2
C0042721  |  viral hepatitis  |  1
C0003467  |  anxiety  |  1
C0026884  |  mutism  |  1
C0014544  |  epilepsy  |  1
C0042373  |  vascular diseases  |  1
C0085543  |  epilepsia partialis continua  |  1
C0014544  |  epilepsia  |  1
C0014544  |  epileptic seizure  |  1
C0014544  |  epileptic seizures  |  1
C0021400  |  influenza  |  1
C0679466  |  cognitive deficits  |  1
C0040053  |  thrombosis  |  1
C0019158  |  hepatitis  |  1
C0004114  |  astrocytoma  |  1
C0026654  |  moyamoya disease  |  1
C0015469  |  facial paralysis  |  1
C0023882  |  spastic diplegia  |  1
C0271355  |  abducens nerve palsy  |  1
C0004936  |  mental disorders  |  1
C0002871  |  anemia  |  1
C0007274  |  carotid artery thrombosis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:3)
ATP1A2  |  477  |  GHR
ATP1A3  |  478  |  GHR
CGA  |  1081  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:176)
5009  |  OTC  |  DISEASES
7544  |  ZFY  |  DISEASES
10857  |  PGRMC1  |  DISEASES
2158  |  F9  |  DISEASES
5327  |  PLAT  |  DISEASES
268  |  AMH  |  DISEASES
2798  |  GNRHR  |  DISEASES
5250  |  SLC25A3  |  DISEASES
55856  |  ACOT13  |  DISEASES
3485  |  IGFBP2  |  DISEASES
22868  |  FASTKD2  |  DISEASES
79441  |  HAUS3  |  DISEASES
5740  |  PTGIS  |  DISEASES
583  |  BBS2  |  DISEASES
6662  |  SOX9  |  DISEASES
3630  |  INS  |  DISEASES
7837  |  PXDN  |  DISEASES
6117  |  RPA1  |  DISEASES
182  |  JAG1  |  DISEASES
1022  |  CDK7  |  DISEASES
7252  |  TSHB  |  DISEASES
63982  |  ANO3  |  DISEASES
3569  |  IL6  |  DISEASES
29113  |  C6orf15  |  DISEASES
6496  |  SIX3  |  DISEASES
1800  |  DPEP1  |  DISEASES
443  |  ASPA  |  DISEASES
4854  |  NOTCH3  |  DISEASES
10000  |  AKT3  |  DISEASES
5443  |  POMC  |  DISEASES
2121  |  EVC  |  DISEASES
6507  |  SLC1A3  |  DISEASES
54504  |  CPVL  |  DISEASES
8034  |  SLC25A16  |  DISEASES
23710  |  GABARAPL1  |  DISEASES
11081  |  KERA  |  DISEASES
51411  |  BIN2  |  DISEASES
79944  |  L2HGDH  |  DISEASES
5373  |  PMM2  |  DISEASES
7157  |  TP53  |  DISEASES
148327  |  CREB3L4  |  DISEASES
4851  |  NOTCH1  |  DISEASES
5741  |  PTH  |  DISEASES
3192  |  HNRNPU  |  DISEASES
9510  |  ADAMTS1  |  DISEASES
7508  |  XPC  |  DISEASES
340348  |  TSPAN33  |  DISEASES
3837  |  KPNB1  |  DISEASES
54361  |  WNT4  |  DISEASES
90525  |  SHF  |  DISEASES
57465  |  TBC1D24  |  DISEASES
476  |  ATP1A1  |  DISEASES
10915  |  TCERG1  |  DISEASES
9317  |  PTER  |  DISEASES
140612  |  ZFP28  |  DISEASES
1632  |  ECI1  |  DISEASES
4054  |  LTBP3  |  DISEASES
79058  |  ASPSCR1  |  DISEASES
478  |  ATP1A3  |  DISEASES
6323  |  SCN1A  |  DISEASES
7543  |  ZFX  |  DISEASES
11141  |  IL1RAPL1  |  DISEASES
23636  |  NUP62  |  DISEASES
2525  |  FUT3  |  DISEASES
5066  |  PAM  |  DISEASES
695  |  BTK  |  DISEASES
84153  |  RNASEH2C  |  DISEASES
2147  |  F2  |  DISEASES
5340  |  PLG  |  DISEASES
5626  |  PROP1  |  DISEASES
8557  |  TCAP  |  DISEASES
133522  |  PPARGC1B  |  DISEASES
6844  |  VAMP2  |  DISEASES
7915  |  ALDH5A1  |  DISEASES
3556  |  IL1RAP  |  DISEASES
8575  |  PRKRA  |  DISEASES
6863  |  TAC1  |  DISEASES
10611  |  PDLIM5  |  DISEASES
23017  |  FAIM2  |  DISEASES
25915  |  NDUFAF3  |  DISEASES
2535  |  FZD2  |  DISEASES
55553  |  SOX6  |  DISEASES
26230  |  TIAM2  |  DISEASES
255324  |  EPGN  |  DISEASES
926  |  CD8B  |  DISEASES
796  |  CALCA  |  DISEASES
4692  |  NDN  |  DISEASES
10052  |  GJC1  |  DISEASES
2774  |  GNAL  |  DISEASES
2152  |  F3  |  DISEASES
79621  |  RNASEH2B  |  DISEASES
3329  |  HSPD1  |  DISEASES
113675  |  SDSL  |  DISEASES
124454  |  EARS2  |  DISEASES
197021  |  LCTL  |  DISEASES
56940  |  DUSP22  |  DISEASES
54898  |  ELOVL2  |  DISEASES
7080  |  NKX2-1  |  DISEASES
27030  |  MLH3  |  DISEASES
23646  |  PLD3  |  DISEASES
55010  |  PARPBP  |  DISEASES
112476  |  PRRT2  |  DISEASES
3785  |  KCNQ2  |  DISEASES
2547  |  XRCC6  |  DISEASES
4151  |  MB  |  DISEASES
5792  |  PTPRF  |  DISEASES
79947  |  DHDDS  |  DISEASES
773  |  CACNA1A  |  DISEASES
1284  |  COL4A2  |  DISEASES
477  |  ATP1A2  |  DISEASES
916  |  CD3E  |  DISEASES
1756  |  DMD  |  DISEASES
56259  |  CTNNBL1  |  DISEASES
7044  |  LEFTY2  |  DISEASES
6993  |  DYNLT1  |  DISEASES
2494  |  NR5A2  |  DISEASES
462  |  SERPINC1  |  DISEASES
480  |  ATP1A4  |  DISEASES
632  |  BGLAP  |  DISEASES
262  |  AMD1  |  DISEASES
10500  |  SEMA6C  |  DISEASES
8036  |  SHOC2  |  DISEASES
3897  |  L1CAM  |  DISEASES
164045  |  HFM1  |  DISEASES
959  |  CD40LG  |  DISEASES
3597  |  IL13RA1  |  DISEASES
25792  |  CIZ1  |  DISEASES
2516  |  NR5A1  |  DISEASES
1269  |  CNR2  |  DISEASES
8518  |  IKBKAP  |  DISEASES
4855  |  NOTCH4  |  DISEASES
8242  |  KDM5C  |  DISEASES
114769  |  CARD16  |  DISEASES
1282  |  COL4A1  |  DISEASES
10006  |  ABI1  |  DISEASES
7088  |  TLE1  |  DISEASES
6520  |  SLC3A2  |  DISEASES
2710  |  GK  |  DISEASES
190  |  NR0B1  |  DISEASES
4112  |  MAGEB1  |  DISEASES
4113  |  MAGEB2  |  DISEASES
170302  |  ARX  |  DISEASES
5422  |  POLA1  |  DISEASES
1761  |  DMRT1  |  DISEASES
4155  |  MBP  |  DISEASES
6736  |  SRY  |  DISEASES
51520  |  LARS  |  DISEASES
100131390  |  SP9  |  DISEASES
4905  |  NSF  |  DISEASES
64072  |  CDH23  |  DISEASES
25974  |  MMACHC  |  DISEASES
643418  |  LIPN  |  DISEASES
6335  |  SCN9A  |  DISEASES
340351  |  AGBL3  |  DISEASES
6916  |  TBXAS1  |  DISEASES
8831  |  SYNGAP1  |  DISEASES
4152  |  MBD1  |  DISEASES
116228  |  COX20  |  DISEASES
8522  |  GAS7  |  DISEASES
6513  |  SLC2A1  |  DISEASES
9217  |  VAPB  |  DISEASES
374308  |  PTCHD3  |  DISEASES
85476  |  GFM1  |  DISEASES
111  |  ADCY5  |  DISEASES
10687  |  PNMA2  |  DISEASES
3347  |  HTN3  |  DISEASES
56  |  ACRV1  |  DISEASES
100463289  |  MTRNR2L5  |  DISEASES
930  |  CD19  |  DISEASES
83695  |  RHNO1  |  DISEASES
84525  |  HOPX  |  DISEASES
29115  |  SAP30BP  |  DISEASES
102723508  |  KANTR  |  DISEASES
79104  |  MEG8  |  DISEASES
9597  |  SMAD5-AS1  |  DISEASES
654321  |  SNORA75  |  DISEASES
Locus(Waiting for update.)
Disease ID 1129
Disease hemiplegia
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:45)
HP:0001297  |  Cerebral vascular events  |  70
HP:0012531  |  Pain  |  6
HP:0010628  |  Facial palsy, unilateral or bilateral  |  5
HP:0001257  |  Spasticity  |  4
HP:0100021  |  Cerebral palsy  |  3
HP:0030834  |  Shoulder pain  |  3
HP:0000822  |  Hypertension  |  2
HP:0003470  |  Inability to move  |  2
HP:0002015  |  Swallowing difficulty  |  2
HP:0002076  |  Migraine headaches  |  2
HP:0002381  |  Aphasia  |  2
HP:0001269  |  Hemiparesis  |  2
HP:0007209  |  Facial paresis  |  1
HP:0011134  |  Mild fever  |  1
HP:0001260  |  Dysarthric speech  |  1
HP:0001903  |  Anemia  |  1
HP:0001907  |  Thromboembolic disease  |  1
HP:0002140  |  Ischemic stroke  |  1
HP:0030746  |  Intraventricular hemorrhage  |  1
HP:0001250  |  Seizures  |  1
HP:0012115  |  Liver inflammation  |  1
HP:0006562  |  Viral hepatitis  |  1
HP:0000739  |  Anxiety  |  1
HP:0012847  |  Epilepsia partialis continua  |  1
HP:0100556  |  Hemiatrophy of the body  |  1
HP:0100735  |  Hypertensive crisis  |  1
HP:0001276  |  Hypertonia  |  1
HP:0200026  |  Ocular pain  |  1
HP:0001259  |  Coma  |  1
HP:0000969  |  Dropsy  |  1
HP:0002138  |  Subarachnoid hemorrhage  |  1
HP:0002300  |  Muteness  |  1
HP:0001288  |  Gait disturbance  |  1
HP:0001348  |  Brisk reflexes  |  1
HP:0011986  |  Ectopic bone formation  |  1
HP:0100543  |  Cognitive deficits  |  1
HP:0002427  |  Loss of expressive speech  |  1
HP:0030516  |  Homonymous hemianopia  |  1
HP:0009592  |  Astrocytoma  |  1
HP:0002170  |  Intracranial hemorrhage  |  1
HP:0012444  |  Brain wasting  |  1
HP:0001239  |  Wrist flexion deformity  |  1
HP:0001264  |  Spastic diplegia  |  1
HP:0000975  |  Increased sweating  |  1
HP:0003474  |  Sensory impairment  |  1
Disease ID 1129
Disease hemiplegia
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:8)
C0030193  |  pain  |  6
C0026838  |  spasticity  |  4
C0037011  |  shoulder pain  |  3
C0040053  |  thrombosis  |  1
C0014544  |  epilepsy  |  1
C0023015  |  language disorders  |  1
C0036572  |  seizures  |  1
C0034931  |  shoulder-hand syndrome  |  1
Manually Genotype(Total Text Mining 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.)
Chemical(Total Drugs:10)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0018991baclofenD0014181134-47-0hemiplegiaMESH:D006429therapeutic12917859
C0018991bortezomibD000069286-hemiplegiaMESH:D006429marker/mechanism17204182
C0018991haloperidolD00622052-86-8hemiplegiaMESH:D006429marker/mechanism3683725
C0018991methotrexateD0087271959/5/2hemiplegiaMESH:D006429marker/mechanism12764767
C0018991methylphenidateD008774113-45-1hemiplegiaMESH:D006429marker/mechanism7115156
C0018991morphineD00902057-27-2hemiplegiaMESH:D006429marker/mechanism6692145
C0018991phenytoinD01067257-41-0hemiplegiaMESH:D006429marker/mechanism3117426
C0018991tacrolimusD016559109581-93-3hemiplegiaMESH:D006429marker/mechanism21321342
C0018991tranexamic acidD0141481197-18-8hemiplegiaMESH:D006429marker/mechanism7104262
C0018991vincristineD014750-hemiplegiaMESH:D006429marker/mechanism20363963
FDA approved drug and dosage information(Total Drugs:5)
DiseaseID Drug_name active_ingredients strength Dosage Form/Route Marketing Status TE code RLD RS
MESH:D006429daytranamethylphenidate10MG/9HR (1.1MG/HR)FILM, EXTENDED RELEASE;TRANSDERMALPrescriptionNoneYesNo
MESH:D006429daytranamethylphenidate10MG/9HR (1.1MG/HR)FILM, EXTENDED RELEASE;TRANSDERMALPrescriptionNoneYesNo
MESH:D006429daytranamethylphenidate10MG/9HR (1.1MG/HR)FILM, EXTENDED RELEASE;TRANSDERMALPrescriptionNoneYesNo
MESH:D006429lystedatranexamic acid650MGTABLET;ORALPrescriptionABYesYes
MESH:D006429velcadebortezomib3.5MG/VIALINJECTABLE;INTRAVENOUS, SUBCUTANEOUSPrescriptionNoneYesYes
FDA labeling changes(Total Drugs:5)
DiseaseID Pediatric_Labeling_Date Trade_Name Generic_Name_or_Proper_Name Indications Studied Label Changes Summary Product Labeling BPCA(B) PREA(P) BPCA(B) and PREA(P) Pediatric Rule (R) Sponsor Pediatric Exclusivity Granted Date NNPS
MESH:D0064296/4/2006daytranamethylphenidateADHDSummary is pendingLabeling-P--Shire-FALSE'
MESH:D00642912/14/2009daytranamethylphenidatePostmarketing safety studyInformation added to Warnings and Adverse Reactions on skin reactions observed in a postmarketing dermal study in pediatric patientsLabeling-P--Shire-FALSE'
MESH:D00642906/29/2010daytranamethylphenidateADHDExpanded pediatric indication to include adolescent patients ages13-17 years The most commonly reported adverse reactions in a trial in patients 13-17 years included appetite decreased, nausea, insomnia, weight decreased, dizziness, abdominal pain, and anorexia. The majority of patients had erythema at the application site Information on PK parameters, Adverse Event profile and clinical studiesLabeling-P--Shire-FALSE'
MESH:D00642908/21/2013lystedatranexamic acidTreatment of cyclic heavy menstrual bleedingIndicated for women of reproductive age. It is not intended for use in premenarcheal girls Information on PK studyPostmarketing study-P--Ferring-FALSE'-
MESH:D00642909/14/2015velcadebortezomibRelapsed Acute Lymphoblastic Leukemia (ALL) and Lymphoblastic Lymphoma (LL)Effectiveness in pediatric patients with relapsed pre-B ALL has not been established. The activity and safety of Velcade in combination with intensive reinduction chemotherapy was evaluated in pediatric and young adult patients with lymphoid malignancies. There were 140 patients with ALL or LL enrolled and evaluated for safety. No new safety concerns were observedLabelingB---Millennium Pharmaceuticals, Inc.-FALSE