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Details
Link-It Detail - Disease - DOLICHOCEPHALY
Debug Stats
  • ### Total Build Time: 64 ms 21.309 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 326 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=20 ms Completed: 20 ms rowSize= 2.697 KB
  • CONCEPT_GENES gt=33 ms Completed: 33 ms rowSize= 17.074 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
DOLICHOCEPHALY C0221358
Relationships (4)

Relation Types:
diso_​to_​anat : 1
diso_​to_​diso : 3


Relationships:
associated_​with : 1
isa : 2
location_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATlocation_ofimg Head C0018670
DISO_to_DISOassociated_withimg Abnormally long growth C0332897
DISO_to_DISOisaimg Dolichocephalic dwarfism C0265206
DISO_to_DISOisaimg Scaphycephaly C0265534
Genes (20)

Species:
human : 20
SpeciesGeneGeneIdGene NameEvidence
HumanNSD164324nuclear receptor binding SET domain protein 1
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanPEX2655670peroxisomal biogenesis factor 26
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanDYM54808dymeclin
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanCUL79820cullin 7
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanPREPL9581prolyl endopeptidase-like
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanSNRPN6638small nuclear ribonucleoprotein polypeptide N
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanSLC3A16519solute carrier family 3 (amino acid transporter heavy chain), member 1
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanPEX55830peroxisomal biogenesis factor 5
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanMAP2K25605mitogen-activated protein kinase kinase 2
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanPEX135194peroxisomal biogenesis factor 13
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanPEX105192peroxisomal biogenesis factor 10
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanPEX15189peroxisomal biogenesis factor 1
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanNDN4692necdin, melanoma antigen (MAGE) family member
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanTRIM374591tripartite motif containing 37
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanFBN12200fibrillin 1
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanDLX31747distal-less homeobox 3
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanBRAF673v-raf murine sarcoma viral oncogene homolog B
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanBLM641Bloom syndrome, RecQ helicase-like
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanATRX546alpha thalassemia/mental retardation syndrome X-linked
img OMIM, Score=1000, UMLKSK CUI: C0221358
HumanALPL249alkaline phosphatase, liver/bone/kidney
img OMIM, Score=1000, UMLKSK CUI: C0221358
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0221358DOLICHOCEPHALY0self