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Details
Link-It Detail - Human Phenotype - Abnormality of habitus
Debug Stats
  • ### Total Build Time: 13 ms 22.820 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 197 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=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_NAMESPACE gt=0 Completed: 0 ms rowSize= 168 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 439 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 756 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.154 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 18.981 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.017 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of habitus HP:0010718
Namespace (1)
medical_genetics
Parents (1)
img Growth abnormality HP:0001507
Children (2)
img Eunuchoid habitus HP:0003782
img Slender build HP:0001533
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Growth abnormality HP:0001507
Genes (30)

Species:
human : 30
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSCARF291179scavenger receptor class F, member 2
img HP RolledUp, OMIM ID: 600920
HumanZNF46984627zinc finger protein 469
HumanZDHHC951114zinc finger, DHHC-type containing 9
img HP RolledUp, OMIM ID: 300799
HumanMMVP150951myxomatous mitral valve prolapse 1
HumanNSDHL50814NAD(P) dependent steroid dehydrogenase-like
img HP RolledUp, OMIM ID: 300831
HumanMED129968mediator complex subunit 12
HumanWHSC17468Wolf-Hirschhorn syndrome candidate 1
img HP RolledUp, OMIM ID: 194190
HumanWHCR7467Wolf-Hirschhorn syndrome chromosome region
img HP RolledUp, OMIM ID: 194190
HumanTPM37170tropomyosin 3
img HP RolledUp, OMIM ID: 161800
HumanTPM27169tropomyosin 2 (beta)
img HP RolledUp, OMIM ID: 161800
HumanTGFBR27048transforming growth factor, beta receptor II (70/80kDa)
HumanTGFBR17046transforming growth factor, beta receptor 1
HumanTGFB17040transforming growth factor, beta 1
img HP RolledUp, OMIM ID: 131300
HumanSKI6497v-ski avian sarcoma viral oncogene homolog
img HP RolledUp, OMIM ID: 182212
HumanRET5979ret proto-oncogene
HumanPLOD15351procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
HumanNEB4703nebulin
img HP RolledUp, OMIM ID: 256030
HumanKAL13730Kallmann syndrome 1 sequence
img HP RolledUp, OMIM ID: 308700
HumanHPGD3248hydroxyprostaglandin dehydrogenase 15-(NAD)
HumanGRIA32892glutamate receptor, ionotropic, AMPA 3
img HP RolledUp, OMIM ID: 300699
HumanFBN22201fibrillin 2
HumanFBN12200fibrillin 1
img HP RolledUp, OMIM ID: 604308
img HP RolledUp, OMIM ID: 182212
HumanDNA21763DNA replication helicase/nuclease 2
img HP RolledUp, OMIM ID: 615156
HumanCYP19A11588cytochrome P450, family 19, subfamily A, polypeptide 1
img HP RolledUp, OMIM ID: 613546
HumanCOL6A31293collagen, type VI, alpha 3
img HP RolledUp, OMIM ID: 254090
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010718Abnormality of habitus0self