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Details
Link-It Detail - Human Phenotype - Abnormality of head and neck
Debug Stats
  • ### Total Build Time: 162 ms 26.399 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 203 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 201 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
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 443 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 772 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.158 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=151 ms Completed: 151 ms rowSize= 22.493 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.022 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of head and neck HP:0000152
Definition (1)
An abnormality of `head and neck` (FMA:280881).
Parents (1)
img Phenotypic abnormality HP:0000118
Children (2)
img Abnormality of the head HP:0000234
img Abnormality of the neck HP:0000464
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001183img Phenotypic abnormality HP:0000118
Genes (2312)

Species:
human : 2312
Page Size
Current 25
  Page 1 of 93
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCTRCT29101867602Cataract 29, coralliform
HumanPAURT1101669760Preauricular tag, isolated, autosomal dominant, 1
HumanGLC1P101448070glaucoma 1, open angle, P
img HP RolledUp, OMIM ID: 615141
HumanCORD17101409267cone rod dystrophy 17 (autosomal dominant)
img HP RolledUp, OMIM ID: 615163
HumanUSH1K101180907Usher syndrome 1K (autosomal recessive)
img HP RolledUp, OMIM ID: 614990
HumanECTD7101101771Ectodermal dysplasia 7, hair/nail type
img HP RolledUp, OMIM ID: 614929
HumanECTD5101101769Ectodermal dysplasia 5, hair/nail type
img HP RolledUp, OMIM ID: 614927
HumanECTD8101101768Ectodermal dysplasia 8, hair/tooth/nail type
img HP RolledUp, OMIM ID: 602401
HumanNYS7101055624Nystagmus 7, congenital
img HP RolledUp, OMIM ID: 614826
HumanPDA1100996949Patent ductus arteriosus, susceptibility to
img HP RolledUp, OMIM ID: 607411
HumanDUP16P11.2100909384
img HP RolledUp, OMIM ID: 614671
HumanKTCN7100887822Keratoconus 7
img HP RolledUp, OMIM ID: 614629
HumanDELXQ21100887743Choroideremia, deafness, and mental retardation
HumanKTCN8100885803Keratoconus 8
img HP RolledUp, OMIM ID: 614628
HumanKTCN6100885802Keratoconus 6
img HP RolledUp, OMIM ID: 614623
HumanKTCN5100885801Keratoconus 5
img HP RolledUp, OMIM ID: 614622
HumanOTDD100885788Otodental dysplasia chromsome deletion syndrome
img HP RolledUp, OMIM ID: 166750
HumanDEL8Q12Q21100885787Bor-Duane hydrocephalus contiguous gene syndrome
img HP RolledUp, OMIM ID: 600257
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP RolledUp, OMIM ID: 608156
HumanDYT21100885773dystonia 21, torsion (autosomal dominant)
img HP RolledUp, OMIM ID: 614588
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDUP17Q12100884129Chromosome 17q12 duplication syndrome
img HP RolledUp, OMIM ID: 614526
HumanDUPXQ27.3Q28100874533
img HP RolledUp, OMIM ID: 300869
HumanC16DELQ22100874527Chromosome 16q22 deletion syndrome
img HP RolledUp, OMIM ID: 614541
HumanCATMANS100862706Catel-Manzke syndrome
img HP RolledUp, OMIM ID: 302380
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000152Abnormality of head and neck0self