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Details
Link-It Detail - Human Phenotype - Abnormality of lower lip
Debug Stats
  • ### Total Build Time: 41 ms 29.301 KB
  • CONCEPT_NAME gt=14 ms Completed: 14 ms rowSize= 199 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 200 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=4 ms Completed: 4 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 443 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.035 KB
  • 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=18 ms Completed: 18 ms rowSize= 24.122 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.019 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of lower lip HP:0000178
Definition (1)
An abnormality of the `lower lip` (FMA:59818).
Parents (1)
img Abnormality of the lip HP:0000159
Children (6)
img Lower lip pit HP:0000196
img Cleft lower lip HP:0010281
img Everted lower lip vermilion HP:0000232
img Thick lower lip vermilion HP:0000179
img Thin lower lip vermilion HP:0010282
img Curved linear dimple below the lower lip HP:0002055
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the lip HP:0000159
Genes (116)

Species:
human : 116
Page Size
Current 25
  Page 1 of 5
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL2Q23.1100820633
img HP IEA, OMIM ID: 156200
HumanDEL13Q14100653382Chromosome 13q14 deletion syndrome
img HP RolledUp, OMIM ID: 613884
HumanDEL14Q11Q22100505392Chromosome 14q11-q22 deletion syndrome
img HP RolledUp, OMIM ID: 613457
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanAMMEC100499260Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis
img HP RolledUp, OMIM ID: 300194
HumanRCHTS100462676Roifman-Chitayat syndrome
img HP RolledUp, OMIM ID: 613328
HumanDUPXQ28100415893Chromosome Xq28 duplication syndrome
img HP RolledUp, OMIM ID: 300815
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanMICRODEL3Q29100188788Chromosome 3q29 microdeletion syndrome
img HP RolledUp, OMIM ID: 609425
HumanDEL17Q21.31791085
img HP RolledUp, OMIM ID: 610443
HumanMPDMRS574047Martin-Probst deafness-mental retardation syndrome
img HP RolledUp, OMIM ID: 300519
HumanCDAGS574043Craniosynostosis, anal anomalies, and porokeratosis syndrome
img HP RolledUp, OMIM ID: 603116
HumanZLS353173Zimmerman-Laband Syndrome
img HP RolledUp, OMIM ID: 135500
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
img HP RolledUp, OMIM ID: 610443
HumanRAB40AL282808RAB40A, member RAS oncogene family-like
img HP RolledUp, OMIM ID: 300519
HumanAMER1139285APC membrane recruitment protein 1
img HP RolledUp, OMIM ID: 300373
HumanHGSNAT138050heparan-alpha-glucosaminide N-acetyltransferase
img HP RolledUp, OMIM ID: 252930
HumanEDARADD128178EDAR-associated death domain
img HP RolledUp, OMIM ID: 129490
img HP RolledUp, OMIM ID: 224900
img HP RolledUp, OMIM ID: 614940
img HP RolledUp, OMIM ID: 614941
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanC12orf57113246chromosome 12 open reading frame 57
img HP RolledUp, OMIM ID: 218340
HumanIFT43112752intraflagellar transport 43 homolog (Chlamydomonas)
img HP RolledUp, OMIM ID: 614099
HumanSTRADA92335STE20-related kinase adaptor alpha
img HP RolledUp, OMIM ID: 611087
HumanSCARF291179scavenger receptor class F, member 2
img HP RolledUp, OMIM ID: 600920
HumanANTXR184168anthrax toxin receptor 1
img HP RolledUp, OMIM ID: 230740
HumanCDT181620chromatin licensing and DNA replication factor 1
img HP RolledUp, OMIM ID: 613804
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000178Abnormality of lower lip0self