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Details
Link-It Detail - Human Phenotype - Abnormality of body weight
Debug Stats
  • ### Total Build Time: 54 ms 27.435 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 201 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=1 ms Completed: 1 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= 439 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.063 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.154 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=40 ms Completed: 40 ms rowSize= 23.427 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of body weight HP:0004323
Parents (1)
img Growth abnormality HP:0001507
Children (3)
img Eunuchoid habitus HP:0003782
img Increased body weight HP:0004324
img Decreased body weight HP:0004325
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Growth abnormality HP:0001507
Genes (691)

Species:
human : 691
Page Size
Current 25
  Page 1 of 28
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDELXQ21100887743Choroideremia, deafness, and mental retardation
img HP RolledUp, OMIM ID: 303110
HumanDUPXQ27.3Q28100874533
img HP RolledUp, OMIM ID: 300869
HumanC16DELQ22100874527Chromosome 16q22 deletion syndrome
img HP RolledUp, OMIM ID: 614541
HumanFWS100529224Forsythe-Wakeling syndrome
img HP RolledUp, OMIM ID: 613606
HumanIBD11100529151Inflammatory bowel disease 11
img HP RolledUp, OMIM ID: 191390
HumanDEL11P13100528024Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome
img HP RolledUp, OMIM ID: 194072
HumanOCLN100506658occludin
img HP RolledUp, OMIM ID: 251290
HumanDEL14Q11Q22100505392Chromosome 14q11-q22 deletion syndrome
img HP RolledUp, OMIM ID: 613457
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanEOE2100499167Esophagitis, eosinophilic, 2
img HP RolledUp, OMIM ID: 613412
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP RolledUp, OMIM ID: 606407
HumanDEL17Q23.1Q23.2100415941
img HP RolledUp, OMIM ID: 613355
HumanDUP5P13100379202Chromosome 5p13 duplication syndrome
img HP RolledUp, OMIM ID: 613174
HumanGRD1100312954Graves disease, susceptiblity to, 1
img HP RolledUp, OMIM ID: 275000
HumanDUPXP11.23P11.22100310754
img HP RolledUp, OMIM ID: 300801
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanFL1100306940Follicular lymphoma, susceptibility to, 1
img HP RolledUp, OMIM ID: 613024
HumanEE100302511Esophagitis, eosinophilic
img HP RolledUp, OMIM ID: 610247
HumanDEL15Q26QTER100271921Chromosome 15q26-qter deletion syndrome
img HP RolledUp, OMIM ID: 612626
HumanDEL18P100240747Chromosome 18p deletion syndrome
img HP RolledUp, OMIM ID: 146390
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanDEL11P15P14100240736Chromosome 11p15-p14 deletion syndrome
img HP RolledUp, OMIM ID: 606528
HumanDEL18Q100216483Chromosome 18q deletion syndrome
img HP RolledUp, OMIM ID: 601808
HumanDUP3Q29100188862chromosome 3q29 microduplication syndrome
img HP RolledUp, OMIM ID: 611936
HumanMRT5100188831mental retardation, non-syndromic, autosomal recessive, 5
img HP RolledUp, OMIM ID: 611091
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0004323Abnormality of body weight0self