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Details
Link-It Detail - Disease - Cleft Palate
Debug Stats
  • ### Total Build Time: 52 ms 55.672 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 322 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 226 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= 247 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 990 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 11.853 KB
  • CONCEPT_RELATIONSHIPS gt=30 ms Completed: 30 ms rowSize= 14.856 KB
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 26.038 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Cleft Palate C0008925
Definition (1)
congenital fissure of the soft and/or hard palate, due to faulty fusion.
Semantic Types (2)
Disease or Syndrome (T047)
Congenital Abnormality (T019)
Parents (2)
img Jaw Abnormalities C0022360
img Mouth Abnormalities C0026633
Ancestral Roots
RootRoot Plus OneDepthParent
img Stomatognathic Diseases C0038368img Jaw Diseases C00223624img Jaw Abnormalities C0022360
img Musculoskeletal Diseases C0026857img Jaw Diseases C00223624img Jaw Abnormalities C0022360
img Musculoskeletal Diseases C0026857img Musculoskeletal Abnormalities C01514916img Jaw Abnormalities C0022360
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007687img Jaw Abnormalities C0022360
img Stomatognathic Diseases C0038368img Stomatognathic System Abnormalities C02430575img Jaw Abnormalities C0022360
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007686img Jaw Abnormalities C0022360
img Stomatognathic Diseases C0038368img Stomatognathic System Abnormalities C02430574img Mouth Abnormalities C0026633
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007685img Mouth Abnormalities C0026633
img Stomatognathic Diseases C0038368img Mouth Diseases C00266364img Mouth Abnormalities C0026633
Relationships (157)

Relation Types:
diso_​to_​anat : 29
diso_​to_​chem : 9
diso_​to_​diso : 107
diso_​to_​gene : 1
diso_​to_​phen : 2
diso_​to_​phys : 9


Relationships:
none : 77
associated_​with : 1
classifies : 2
expanded_​form_​of : 1
is_​associated_​anatomic_​site_​of : 3
isa : 2
location_​of : 1
manifestation_​of : 1
mapped_​to : 68
related_​to : 1
Page Size
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  Page 1 of 7
Prior Page
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO1206img CL - Cleft lip C0008924
DISO_to_DISO858img CL - Cleft lip C0008924
DISO_to_PHEN414img genetic aspects C0017399
DISO_to_DISO307img Complication Aspects C1171258
DISO_to_DISO288img Complication Aspects C1171258
DISO_to_PHEN248img genetic aspects C0017399
DISO_to_ANAT108img Maxilla C0024947
DISO_to_DISO93img Abnormalities, Multiple C0000772
DISO_to_ANAT92img Maxilla C0024947
DISO_to_DISO64img Abnormalities, Multiple C0000772
DISO_to_ANAT62img Alveolar Process C0002386
DISO_to_DISO59img Velopharyngeal Insufficiency C0042454
DISO_to_DISO55img Velopharyngeal Insufficiency C0042454
DISO_to_ANAT54img Palate C0700374
DISO_to_ANAT50img Surgical Flaps C0038925
DISO_to_DISO50img chemically induced C0007994
DISO_to_ANAT49img Palate C0700374
DISO_to_CHEM46img IRF Transcription Factors C1564741
DISO_to_CHEM46img Interferon Regulatory Factors C1564741
DISO_to_PHYS46img Development, Maxillofacial C0024960
DISO_to_ANAT44img Alveolar Process C0002386
DISO_to_PHYS44img Development, Maxillofacial C0024960
DISO_to_GENE43img Polymorphism, Single Nucleotide C0752046
DISO_to_DISO42img Ectodermal Dysplasia C0013575
DISO_to_DISO40img chemically induced C0007994
Genes (92)

Species:
human : 92
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanFREM2341640FRAS1 related extracellular matrix protein 2
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanHYLS1219844hydrolethalus syndrome 1
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanPROKR2128674prokineticin receptor 2
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanFRAS180144Fraser syndrome 1
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanFKRP79147fukutin related protein
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanPORCN64840porcupine homolog (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanALX460529ALX homeobox 4
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanFAM20C56975family with sequence similarity 20, member C
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanCHD755636chromodomain helicase DNA binding protein 7
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanMKS154903Meckel syndrome, type 1
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanBCOR54880BCL6 corepressor
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanTBX2250945T-box 22
img GENERIF, Score=660, Pubmed Id: 17868388, UMLKSK CUI: C0008925
img GENERIF, Score=1000, Pubmed Id: 12374769, UMLKSK CUI: C0008925
img GENERIF, Score=694, Pubmed Id: 14729838, UMLKSK CUI: C0008925
HumanPOMT229954protein-O-mannosyltransferase 2
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanSATB223314SATB homeobox 2
img OMIM, Score=1000, UMLKSK CUI: C0008925
img GENERIF, Score=734, Pubmed Id: 12915443, UMLKSK CUI: C0008925
HumanSEPT910801septin 9
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanPOMT110585protein-O-mannosyltransferase 1
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanZMPSTE2410269zinc metallopeptidase STE24
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanCD9610225CD96 molecule
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanPQBP110084polyglutamine binding protein 1
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanARNT29915aryl-hydrocarbon receptor nuclear translocator 2
img GENERIF, Score=901, Pubmed Id: 12210012, UMLKSK CUI: C0008925
HumanSEMA3E9723sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanTBX49496T-box 4
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanRECQL49401RecQ protein-like 4
img OMIM, Score=1000, UMLKSK CUI: C0008925
HumanLARGE9215like-glycosyltransferase
img OMIM, Score=1000, UMLKSK CUI: C0008925
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0008925Cleft Palate0self