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Details
Link-It Detail - Disease - Paresis
Debug Stats
  • ### Total Build Time: 39 ms 33.094 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 312 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 567 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=14 ms Completed: 14 ms rowSize= 184 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 561 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 549 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.819 KB
  • CONCEPT_RELATIONSHIPS gt=7 ms Completed: 7 ms rowSize= 12.821 KB
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 14.162 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.142 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Paresis C0030552
Definition (1)
A general term referring to a mild to moderate degree of muscular weakness, occasionally used as a synonym for PARALYSIS (severe or complete loss of motor function). In the older literature, paresis often referred specifically to paretic neurosyphilis (see NEUROSYPHILIS). "General paresis" and "general paralysis" may still carry that connotation. Bilateral lower extremity paresis is referred to as PARAPARESIS.
Semantic Types (1)
Sign or Symptom (T184)
Parents (1)
img Neurologic Manifestations C0027854
Children (1)
img Paraparesis C0221166
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370884img Neurologic Manifestations C0027854
img Nervous System Diseases C0027765img Neurologic Manifestations C00278543img Neurologic Manifestations C0027854
Relationships (70)

Relation Types:
diso_​to_​anat : 23
diso_​to_​chem : 1
diso_​to_​diso : 33
diso_​to_​phys : 13


Relationships:
none : 62
associated_​with : 5
isa : 1
parent_​is_​cdrh : 1
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO453img Cerebrovascular accident C0038454
DISO_to_DISO211img Cerebrovascular accident C0038454
DISO_to_ANAT80img Arm C0446516
DISO_to_DISO68img Complication Aspects C1171258
DISO_to_DISO67img AMBULATION DIS NEUROLOGIC C0751830
DISO_to_ANAT61img Muscle, Skeletal C0242692
DISO_to_DISO61img Function Recoveries C0599766
DISO_to_ANAT57img Upper Extremity C1140618
DISO_to_ANAT50img Arm C0446516
DISO_to_ANAT44img Cortex, Motor C0026607
DISO_to_ANAT41img Muscle, Skeletal C0242692
DISO_to_PHYS36img Movement C0026649
DISO_to_DISO35img Gait C0016928
DISO_to_PHYS35img Movement C0026649
DISO_to_ANAT34img Hand C0018563
DISO_to_PHYS34img Functional Laterality C1720777
DISO_to_DISO33img Movement Disorders C0026650
DISO_to_DISO30img Function Recoveries C0599766
DISO_to_ANAT29img Leg C1140621
DISO_to_DISO27img Complication Aspects C1171258
DISO_to_PHYS27img Balance, Postural C1256755
DISO_to_DISO26img Muscle Spasticity C0026838
DISO_to_PHYS24img Performance, Psychomotor C0033923
DISO_to_PHYS21img Functional Laterality C1720777
DISO_to_PHYS21img Performance, Psychomotor C0033923
Genes (22)

Species:
human : 22
SpeciesGeneGeneIdGene NameEvidence
HumanPDB494003Paget disease of bone 4
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanSPG1180208spastic paraplegia 11 (autosomal recessive)
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanFA2H79152fatty acid 2-hydroxylase
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanGJC257165gap junction protein, gamma 2, 47kDa
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanSPG2151324spastic paraplegia 21 (autosomal recessive, Mast syndrome)
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanHSPB826353heat shock 22kDa protein 8
img OMIM, Score=1000, UMLKSK CUI: C0030552
HumanSLC25A1510166solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanSQSTM18878sequestosome 1
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanTNFRSF11A8792tumor necrosis factor receptor superfamily, member 11a, NFKB activator
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanSPG76687spastic paraplegia 7 (pure and complicated autosomal recessive)
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanSPAST6683spastin
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanSOX106663SRY (sex determining region Y)-box 10
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanPSEN15663presenilin 1
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanNF14763neurofibromin 1
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanHSPD13329heat shock 60kDa protein 1 (chaperonin)
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanHSPB13315heat shock 27kDa protein 1
img OMIM, Score=1000, UMLKSK CUI: C0030552
HumanGJB12705gap junction protein, beta 1, 32kDa
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanGJA12697gap junction protein, alpha 1, 43kDa
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanGBA2629glucosidase, beta, acid
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanEDNRB1910endothelin receptor type B
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanEDN31908endothelin 3
INFERRED, Score=800, UMLKSK CUI: C0030552
HumanCA2760carbonic anhydrase II
img OMIM, Score=790, UMLKSK CUI: C0030552
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0030552Paresis0self