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Details
Link-It Detail - Human Phenotype - Abnormality of the nipple
Debug Stats
  • ### Total Build Time: 37 ms 27.937 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 200 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 197 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=6 ms Completed: 6 ms rowSize= 446 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 2.021 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.161 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 22.767 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.020 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the nipple HP:0004404
Definition (1)
An abnormality of the `nipple` (FMA:67771).
Parents (1)
img Abnormality of the breast HP:0000769
Children (6)
img Prominent nipples HP:0004405
img Aplasia/Hypoplasia of the nipples HP:0006709
img Low-set nipples HP:0002562
img Wide intermamillary distance HP:0006610
img Supernumerary nipples HP:0002558
img Inverted nipples HP:0003186
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the breast HP:0000769
Genes (91)

Species:
human : 91
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP TAS, OMIM ID: 608156
HumanC16DELQ22100874527Chromosome 16q22 deletion syndrome
img HP RolledUp, OMIM ID: 614541
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP TAS, OMIM ID: 252270
HumanDEL17P13.1100653374
img HP RolledUp, OMIM ID: 613776
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP TAS, OMIM ID: 158170
HumanDEL18P100240747Chromosome 18p deletion syndrome
img HP TAS, OMIM ID: 146390
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanCFSS100188773craniofacioskeletal syndrome
img HP RolledUp, OMIM ID: 300712
HumanAOS100188340Adams-Oliver syndrome
img HP RolledUp, OMIM ID: 100300
HumanDEL17Q21.31791085
img HP RolledUp, OMIM ID: 610443
HumanTQDS780911Chromosome 10q deletion syndrome
img HP RolledUp, OMIM ID: 609625
HumanMPDMRS574047Martin-Probst deafness-mental retardation syndrome
img HP RolledUp, OMIM ID: 300519
HumanALG11440138ALG11, alpha-1,2-mannosyltransferase
img HP RolledUp, OMIM ID: 613661
HumanGDF6392255growth differentiation factor 6
img HP TAS, OMIM ID: 118100
HumanFREM2341640FRAS1 related extracellular matrix protein 2
img HP TAS, OMIM ID: 219000
HumanKCTD1284252potassium channel tetramerization domain containing 1
img HP RolledUp, OMIM ID: 181270
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
img HP RolledUp, OMIM ID: 610443
HumanRAB40AL282808RAB40A, member RAS oncogene family-like
img HP RolledUp, OMIM ID: 300519
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP RolledUp, OMIM ID: 605039
HumanB3GALTL145173beta 1,3-galactosyltransferase-like
img HP TAS, OMIM ID: 261540
HumanAMER1139285APC membrane recruitment protein 1
img HP RolledUp, OMIM ID: 300373
HumanEDARADD128178EDAR-associated death domain
img HP RolledUp, OMIM ID: 614940
img HP RolledUp, OMIM ID: 614941
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0004404Abnormality of the nipple0self