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Details
Link-It Detail - Human Phenotype - Abnormality of the myocardium
Debug Stats
  • ### Total Build Time: 63 ms 27.398 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 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=4 ms Completed: 4 ms rowSize= 464 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.057 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.179 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=36 ms Completed: 36 ms rowSize= 23.343 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.023 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the myocardium HP:0001637
Parents (1)
img Malformation of the heart and great vessels HP:0002564
Children (3)
img Myocardial fibrosis HP:0001685
img Myocardial necrosis HP:0001700
img Cardiomyopathy HP:0001638
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Malformation of the heart and great vessels HP:0002564
Genes (276)

Species:
human : 276
Page Size
Current 25
  Page 1 of 12
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMYMY4100653379Moyamoya disease 4
img HP RolledUp, OMIM ID: 300845
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanCFTDX100188765Myopathy, congenital, with fiber-type disproportion, X-linked
img HP RolledUp, OMIM ID: 300580
HumanD2HGDH728294D-2-hydroxyglutarate dehydrogenase
img HP RolledUp, OMIM ID: 600721
HumanSDHAF1644096succinate dehydrogenase complex assembly factor 1
img HP RolledUp, OMIM ID: 252011
HumanCOA5493753cytochrome c oxidase assembly factor 5
img HP RolledUp, OMIM ID: 220110
HumanBOLA3388962bolA family member 3
img HP RolledUp, OMIM ID: 614299
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
img HP RolledUp, OMIM ID: 203300
HumanLCRB387281locus control region, beta
img HP RolledUp, OMIM ID: 613985
HumanZLS353173Zimmerman-Laband Syndrome
img HP RolledUp, OMIM ID: 135500
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img HP RolledUp, OMIM ID: 130650
HumanRBM20282996RNA binding motif protein 20
img HP RolledUp, OMIM ID: 613172
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanHFE2148738hemochromatosis type 2 (juvenile)
img HP RolledUp, OMIM ID: 602390
HumanHGSNAT138050heparan-alpha-glucosaminide N-acetyltransferase
img HP RolledUp, OMIM ID: 252930
HumanDNAJC19131118DnaJ (Hsp40) homolog, subfamily C, member 19
img HP RolledUp, OMIM ID: 610198
HumanNDUFA11126328NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 11, 14.7kDa
img HP RolledUp, OMIM ID: 252010
HumanCALR3125972calreticulin 3
img HP RolledUp, OMIM ID: 613875
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanMGME192667mitochondrial genome maintenance exonuclease 1
img HP RolledUp, OMIM ID: 615084
HumanCOG791949component of oligomeric golgi complex 7
img HP RolledUp, OMIM ID: 608779
HumanNDUFAF291942NADH dehydrogenase (ubiquinone) complex I, assembly factor 2
img HP RolledUp, OMIM ID: 252010
HumanATPAF291647ATP synthase mitochondrial F1 complex assembly factor 2
img HP RolledUp, OMIM ID: 604273
HumanNEXN91624nexilin (F actin binding protein)
img HP RolledUp, OMIM ID: 613122
HumanHPS489781Hermansky-Pudlak syndrome 4
img HP RolledUp, OMIM ID: 203300
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001637Abnormality of the myocardium0self