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Details
Link-It Detail - Disease - Melkersson-Rosenthal Syndrome
Debug Stats
  • ### Total Build Time: 17 ms 14.492 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 356 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 555 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 989 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 2.778 KB
  • CONCEPT_RELATIONSHIPS gt=7 ms Completed: 7 ms rowSize= 8.433 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Melkersson-Rosenthal Syndrome C0025235
Definition (1)
An idiopathic syndrome characterized by one or more of the following; recurrent orofacial swelling, relapsing facial paralysis, and fissured tongue (lingua plicata). The onset is usually in childhood and relapses are common. Cheilitis granulomatosa is a monosymptomatic variant of this condition. (Dermatol Clin 1996 Apr;14(2):371-9; Magalini & Magalini, Dictionary of Medical Syndromes, 4th ed, p531)
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Mouth Diseases C0026636
img Facial Nerve Diseases C0015464
Ancestral Roots
RootRoot Plus OneDepthParent
img Stomatognathic Diseases C0038368img Mouth Diseases C00266363img Mouth Diseases C0026636
img Nervous System Diseases C0027765img Cranial Nerve Diseases C00102664img Facial Nerve Diseases C0015464
Relationships (19)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 17


Relationships:
none : 8
associated_​with : 1
location_​of : 1
manifestation_​of : 8
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO16img Complication Aspects C1171258
DISO_to_DISO13img Complication Aspects C1171258
DISO_to_ANAT9img Lip C0023759
DISO_to_DISO7img Edema C0013604
DISO_to_DISO6img A-760-766 DISORDERS OF THE EYELIDS C0015423
DISO_to_DISO6img Cheilitis C0007971
DISO_to_DISO6img Crohn Disease C0010346
DISO_to_DISO6img Facial Paralysis C0015469
DISO_to_ANATlocation_ofimg Lower lip structure C0458583
DISO_to_DISOassociated_withimg 44 GRANULOMATOUS INFLAMMATIONS C0553697
DISO_to_DISOmanifestation_ofimg Facial edema C0542571
DISO_to_DISOmanifestation_ofimg Fissured tongue C0040412
DISO_to_DISOmanifestation_ofimg Granulomatous lymphangitis on eyelid biopsy C1835037
DISO_to_DISOmanifestation_ofimg Insidious, painless, nonpitting eyelid edema C1835035
DISO_to_DISOmanifestation_ofimg LIP SWELLING C0240211
DISO_to_DISOpermuted_term_ofimg Melkersson-Rosenthal Syndrome C0025235
DISO_to_DISOmanifestation_ofimg Onset in childhood or youth C1835038
DISO_to_DISOmanifestation_ofimg Periorbital heterogeneous thickening on CT scan C1835036
DISO_to_DISOmanifestation_ofimg Recurrent peripheral facial palsy LABORATORY : C3149630
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0025235Melkersson-Rosenthal Syndrome0self