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Details
Link-It Detail - Human Phenotype - Abnormality of the endocrine system
Debug Stats
  • ### Total Build Time: 57 ms 30.917 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 210 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 206 bytes
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  • CONCEPT_GENES gt=45 ms Completed: 45 ms rowSize= 23.400 KB
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  • Reload Stats
Human Phenotype (1)
Abnormality of the endocrine system HP:0000818
Definition (1)
Ab abnormality of the `endocrine system` (FMA:9668).
Parents (1)
img Phenotypic abnormality HP:0000118
Children (13)
img Abnormality of the hypothalamus-pituitary axis HP:0000864
img Abnormality of the parathyroid gland HP:0000828
img Hyperinsulinemia HP:0000842
img Diabetes insipidus HP:0000873
img Abnormality of the thyroid gland HP:0000820
img Diabetes mellitus HP:0000819
img Hypertension HP:0000822
img Abnormality of renin-angiotensin system HP:0000847
img Abnormality of circulating hormone level HP:0003117
img Neoplasm of the endocrine system HP:0100568
img Abnormality of the adrenal glands HP:0000834
img Puberty and gonadal disorders HP:0008373
img Abnormality of urine hormone level HP:0012029
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001183img Phenotypic abnormality HP:0000118
Genes (738)

Species:
human : 738
Page Size
Current 25
  Page 1 of 30
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDUPXQ27.3Q28100874533
img HP RolledUp, OMIM ID: 300869
HumanGFND1100689213Glomerulopathy with fibronectin deposits 1
img HP RolledUp, OMIM ID: 137950
HumanDFNB81100653390deafness, autosomal recessive 81
img HP RolledUp, OMIM ID: 614129
HumanIGAN2100653384IgA nephropathy, susceptibility to, 2
img HP RolledUp, OMIM ID: 613944
HumanMYMY4100653379Moyamoya disease 4
img HP RolledUp, OMIM ID: 300845
HumanSRXX210065337846XX sex reversal 2
img HP RolledUp, OMIM ID: 278850
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP RolledUp, OMIM ID: 606407
HumanGRD1100312954Graves disease, susceptiblity to, 1
img HP RolledUp, OMIM ID: 275000
HumanDUPXP11.23P11.22100310754
img HP RolledUp, OMIM ID: 300801
HumanDEL18P100240747Chromosome 18p deletion syndrome
img HP RolledUp, OMIM ID: 146390
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
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
HumanHPRHP100188880Hypophosphatemic rickets and hyperparathyroidism
img HP RolledUp, OMIM ID: 612089
HumanENDO1100188863Endometriosis, susceptibility to, 1
img HP RolledUp, OMIM ID: 131200
HumanAUTS1100188832Autism, susceptibility to, 1
img HP RolledUp, OMIM ID: 209850
HumanHYT6100188808Hypertension, essential, susceptibility to, 6
img HP RolledUp, OMIM ID: 145500
HumanHYT5100188807Hypertension, essential, susceptibility to, 5
img HP RolledUp, OMIM ID: 145500
HumanNIDDM4100188782Diabetes mellitus, noninsulin-dependent
img HP RolledUp, OMIM ID: 125853
HumanKCNJ18100134444potassium inwardly-rectifying channel, subfamily J, member 18
img HP RolledUp, OMIM ID: 613239
HumanPTLS100038247Potocki-Lupski syndrome
img HP RolledUp, OMIM ID: 610883
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000818Abnormality of the endocrine system0self