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Details
Link-It Detail - Disease - Reflex, Abnormal
Debug Stats
  • ### Total Build Time: 90 ms 37.011 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 330 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 313 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=0 Completed: 0 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=1 ms Completed: 1 ms rowSize= 554 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.819 KB
  • CONCEPT_RELATIONSHIPS gt=68 ms Completed: 68 ms rowSize= 13.641 KB
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 17.477 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Reflex, Abnormal C0034933
Definition (1)
An abnormal response to a stimulus applied to the sensory components of the nervous system. This may take the form of increased, decreased, or absent reflexes.
Semantic Types (1)
Sign or Symptom (T184)
Parents (1)
img Neurologic Manifestations C0027854
Children (1)
img Reflex, Babinski C0034935
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 (206)

Relation Types:
diso_​to_​anat : 14
diso_​to_​chem : 1
diso_​to_​diso : 169
diso_​to_​phen : 2
diso_​to_​phys : 20


Relationships:
none : 48
classifies : 2
entry_​version_​of : 1
isa : 9
mapped_​to : 146
Page Size
Current 25
  Page 1 of 9
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHYS120img physiological aspects C0031843
DISO_to_PHYS116img physiological aspects C0031843
DISO_to_ANAT25img Muscle, Skeletal C0242692
DISO_to_PHEN18img genetic aspects C0017399
DISO_to_DISO16img Spinal Cord Injuries C0037929
DISO_to_PHYS16img Baroreflex C0206162
DISO_to_PHYS16img Startle Reaction C0038186
DISO_to_ANAT14img Trigeminal Nerve C0040996
DISO_to_ANAT13img Muscle, Skeletal C0242692
DISO_to_PHYS12img Blinked C0005757
DISO_to_ANAT11img Trigeminal Nerve C0040996
DISO_to_DISO11img Spinal Cord Injuries C0037929
DISO_to_PHEN9img genetic aspects C0017399
DISO_to_PHYS9img Baroreceptor Reflex C0206162
DISO_to_PHYS9img Muscle spindle reflex C0034942
DISO_to_ANAT8img Urinary Bladder C0005682
DISO_to_DISO8img Cerebrovascular accident C0038454
DISO_to_DISO7img Autonomic Nervous System Diseases C1145628
DISO_to_DISO7img Muscle Hypertonia C0026826
DISO_to_DISO7img Muscle Spasticity C0026838
DISO_to_DISO7img Neurogenic Urinary Bladder C0005697
DISO_to_PHYS7img Reflex, Vestibulo-Ocular C0034944
DISO_to_ANAT6img Anal Canal C0227411
DISO_to_ANAT6img Brain C0006104
DISO_to_ANAT6img Brain Stem C0006121
Genes (64)

Species:
human : 64
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNIPA1123606non imprinted in Prader-Willi/Angelman syndrome 1
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanNDUFAF291942NADH dehydrogenase (ubiquinone) complex I, assembly factor 2
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanFAM126A84668family with sequence similarity 126, member A
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanSPG1180208spastic paraplegia 11 (autosomal recessive)
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanC20orf779133
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanMCOLN157192mucolipin 1
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanGJC257165gap junction protein, gamma 2, 47kDa
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanTREM254209triggering receptor expressed on myeloid cells 2
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanATL151062atlastin GTPase 1
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanNDUFAF429078NADH dehydrogenase (ubiquinone) complex I, assembly factor 4
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanBSCL226580Berardinelli-Seip congenital lipodystrophy 2 (seipin)
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanSACS26278spastic ataxia of Charlevoix-Saguenay (sacsin)
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanCHMP2B25978charged multivesicular body protein 2B
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanPLEKHG425894pleckstrin homology domain containing, family G (with RhoGef domain) member 4
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanFBXO725793F-box protein 7
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanZFYVE2623503zinc finger, FYVE domain containing 26
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanATP13A223400ATPase type 13A2
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanSPG2023111spastic paraplegia 20 (Troyer syndrome)
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanSETX23064senataxin
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanCCT522948chaperonin containing TCP1, subunit 5 (epsilon)
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanMFN29927mitofusin 2
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanKIAA01969897KIAA0196
INFERRED, Score=800, UMLKSK CUI: C0034933
HumanCYP7B19420cytochrome P450, family 7, subfamily B, polypeptide 1
INFERRED, Score=800, UMLKSK CUI: C0034933
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0034933Reflex, Abnormal0self