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Details
Link-It Detail - Disease - Facial Paralysis
Debug Stats
  • ### Total Build Time: 42 ms 30.827 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= 332 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=1 ms Completed: 1 ms rowSize= 184 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 977 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 4.054 KB
  • CONCEPT_RELATIONSHIPS gt=29 ms Completed: 29 ms rowSize= 14.150 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 9.657 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Facial Paralysis C0015469
Definition (1)
Partial or complete paralysis of the facial muscles of one side of a person's face. It is caused by damage to the seventh cranial nerve. It is usually temporary but it may recur.
Semantic Types (1)
Sign or Symptom (T184)
Parents (2)
img Mouth Diseases C0026636
img Paralysis C0522224
Ancestral Roots
RootRoot Plus OneDepthParent
img Stomatognathic Diseases C0038368img Mouth Diseases C00266363img Mouth Diseases C0026636
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370885img Paralysis C0522224
img Nervous System Diseases C0027765img Neurologic Manifestations C00278544img Paralysis C0522224
Relationships (83)

Relation Types:
diso_​to_​anat : 22
diso_​to_​chem : 15
diso_​to_​diso : 44
diso_​to_​phen : 1
diso_​to_​phys : 1


Relationships:
none : 57
is_​associated_​anatomic_​site_​of : 1
is_​finding_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 2
isa : 5
mapped_​to : 4
may_​treat : 11
parent_​is_​cdrh : 1
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT125img Facial Nerve C0015462
DISO_to_ANAT81img Facial Nerve C0015462
DISO_to_DISO73img Complication Aspects C1171258
DISO_to_DISO67img Complication Aspects C1171258
DISO_to_DISO64img Facial Nerve Diseases C0015464
DISO_to_DISO51img COMPL POSTOP C0032787
DISO_to_DISO46img Facial Nerve Injuries C0161408
DISO_to_ANAT42img Facial Muscles C0015460
DISO_to_ANAT38img Muscle, Skeletal C0242692
DISO_to_DISO36img COMPL POSTOP C0032787
DISO_to_DISO36img Facial Nerve Diseases C0015464
DISO_to_DISO33img Acoustic Neuroma C0027859
DISO_to_DISO32img CRANIAL NERVE VII INJ C0161408
DISO_to_DISO30img Expression, Facial C0015457
DISO_to_ANAT28img Surgical Flaps C0038925
DISO_to_ANAT26img Hypoglossal Nerve C0020614
DISO_to_ANAT26img Muscle, Skeletal C0242692
DISO_to_ANAT26img Temporal Bone C0039484
DISO_to_DISO26img A-760-766 DISORDERS OF THE EYELIDS C0015423
DISO_to_DISO26img Acoustic Neuroma C0027859
DISO_to_ANAT25img Eyelid structure C0015426
DISO_to_DISO25img A-760-766 DISORDERS OF THE EYELIDS C0015423
DISO_to_ANAT24img Surgical Flaps C0038925
DISO_to_ANAT23img Eyelid structure C0015426
DISO_to_ANAT23img Facial Muscles C0015460
Genes (9)

Species:
human : 9
SpeciesGeneGeneIdGene NameEvidence
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
img OMIM, Score=1000, UMLKSK CUI: C0015469
HumanCHD755636chromodomain helicase DNA binding protein 7
img OMIM, Score=1000, UMLKSK CUI: C0015469
HumanSOST50964sclerostin
img OMIM, Score=1000, UMLKSK CUI: C0015469
img OMIM, Score=1000, UMLKSK CUI: C0015469
HumanOSTM128962osteopetrosis associated transmembrane protein 1
img OMIM, Score=1000, UMLKSK CUI: C0015469
HumanTCIRG110312T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
img OMIM, Score=1000, UMLKSK CUI: C0015469
HumanSEMA3E9723sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
img OMIM, Score=1000, UMLKSK CUI: C0015469
HumanTNFSF118600tumor necrosis factor (ligand) superfamily, member 11
img OMIM, Score=1000, UMLKSK CUI: C0015469
HumanEYA12138eyes absent homolog 1 (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0015469
HumanCLCN71186chloride channel, voltage-sensitive 7
img OMIM, Score=1000, UMLKSK CUI: C0015469
img OMIM, Score=1000, UMLKSK CUI: C0015469
img OMIM, Score=1000, UMLKSK CUI: C0015469
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0015469Facial Paralysis0self