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Details
Link-It Detail - Human Phenotype - Abnormality of the middle ear
Debug Stats
  • ### Total Build Time: 51 ms 31.076 KB
  • CONCEPT_NAME gt=15 ms Completed: 15 ms rowSize= 204 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
  • 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=12 ms Completed: 12 ms rowSize= 3.665 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.082 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=23 ms Completed: 23 ms rowSize= 23.529 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.023 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the middle ear HP:0000370
Parents (1)
img Abnormality of the ear HP:0000598
Children (11)
img Aplasia/Hypoplasia of the middle ear HP:0008773
img Cholesteatoma HP:0009797
img Otitis media HP:0000388
img Abnormality of the middle ear ossicles HP:0004452
img Functional abnormality of the middle ear HP:0011452
img Otosclerosis HP:0000362
img Conductive hearing impairment HP:0000405
img Morphological abnormality of the middle ear HP:0008609
img Neoplasia of the middle ear HP:0100799
img Stapes ankylosis HP:0000381
img Abnormal middle ear reflexes HP:0004454
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the ear HP:0000598
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the ear HP:0000598
Genes (240)

Species:
human : 240
Page Size
Current 25
  Page 1 of 10
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDELXQ21100887743Choroideremia, deafness, and mental retardation
img HP RolledUp, OMIM ID: 303110
HumanCATMANS100862706Catel-Manzke syndrome
img HP RolledUp, OMIM ID: 302380
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL16P12.1P11.2100526742
img HP RolledUp, OMIM ID: 613604
HumanDEL17Q23.1Q23.2100415941
img HP RolledUp, OMIM ID: 613355
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanDEL15Q15.3100240731
img HP RolledUp, OMIM ID: 611102
HumanDEL18Q100216483Chromosome 18q deletion syndrome
img HP RolledUp, OMIM ID: 601808
HumanOTSC8100151644otosclerosis 8
img HP RolledUp, OMIM ID: 612096
HumanSHFM3100049542Split-hand/foot malformation 3
img HP RolledUp, OMIM ID: 246560
HumanAA1100034700Alopecia areata 1
img HP RolledUp, OMIM ID: 104000
HumanAUNX1751798auditory neuropathy, X-linked recessive 1
img HP RolledUp, OMIM ID: 300614
HumanDFNB68751609deafness, autosomal recessive 68
img HP RolledUp, OMIM ID: 610419
HumanOMS619538otitis media, susceptibility to
img HP RolledUp, OMIM ID: 166760
HumanWG474168Wegener granulomatosis
img HP RolledUp, OMIM ID: 608710
HumanDFNB46449488deafness, autosomal recessive 46
img HP RolledUp, OMIM ID: 609647
HumanDFNB51448963deafness, autosomal recessive 51
img HP RolledUp, OMIM ID: 609941
HumanLRSL406214Larsen-like syndrome
img HP RolledUp, OMIM ID: 608545
HumanOTSC7399516otosclerosis 7
img HP RolledUp, OMIM ID: 611572
HumanGDF6392255growth differentiation factor 6
img HP RolledUp, OMIM ID: 118100
img HP RolledUp, OMIM ID: 214300
img HP RolledUp, OMIM ID: 148900
HumanDFNB40379003deafness, autosomal recessive 40
img HP RolledUp, OMIM ID: 608264
HumanDNAAF3352909dynein, axonemal, assembly factor 3
img HP RolledUp, OMIM ID: 606763
HumanFREM2341640FRAS1 related extracellular matrix protein 2
img HP RolledUp, OMIM ID: 219000
HumanCCDC39339829coiled-coil domain containing 39
img HP RolledUp, OMIM ID: 613807
HumanDFNB38337991deafness, autosomal recessive 38
img HP RolledUp, OMIM ID: 608219
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000370Abnormality of the middle ear0self