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Details
Link-It Detail - Human Phenotype - Abnormality of the adrenal glands
Debug Stats
  • ### Total Build Time: 30 ms 30.791 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 208 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 267 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=7 ms Completed: 7 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= 456 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 3.978 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.171 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 23.562 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the adrenal glands HP:0000834
Definition (1)
Abnormality of the `adrenal glands` (FMA:9604), i.e., of the endocrine glands located at the top of the kindneys.
Parents (1)
img Abnormality of the endocrine system HP:0000818
Children (12)
img Adrenocortical abnormality HP:0000849
img Macronodular adrenal hyperplasia HP:0008231
img Abnormality of adrenal physiology HP:0011733
img Adrenal calcification HP:0010512
img Pseudohypoaldosteronism HP:0008242
img Adrenal hypoplasia HP:0000835
img Adrenal hyperplasia HP:0008221
img Adrenal insufficiency HP:0000846
img Mineralocorticoid insufficiency HP:0008190
img Adrenal gland dysgenesis HP:0008216
img Congenital adrenal hyperplasia HP:0008258
img Abnormality of adrenal morphology HP:0011732
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the endocrine system HP:0000818
Genes (127)

Species:
human : 127
Page Size
Current 25
  Page 1 of 6
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
HumanNKCD780917Natural killer cell deficiency, familial isolated
img HP RolledUp, OMIM ID: 609981
HumanLCRB387281locus control region, beta
img HP RolledUp, OMIM ID: 613985
HumanSNORD115-1338433
img HP RolledUp, OMIM ID: 176270
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img HP TAS, OMIM ID: 130650
HumanHYLS1219844hydrolethalus syndrome 1
img HP RolledUp, OMIM ID: 236680
HumanPWAR1145624Prader Willi/Angelman region RNA 1
img HP RolledUp, OMIM ID: 176270
HumanANTXR2118429anthrax toxin receptor 2
img HP TAS, OMIM ID: 236490
HumanHPE6117190holoprosencephaly 6
img HP RolledUp, OMIM ID: 236100
HumanLHX489884LIM homeobox 4
img HP RolledUp, OMIM ID: 262700
HumanWNK465266WNK lysine deficient protein kinase 4
img HP RolledUp, OMIM ID: 601844
img HP RolledUp, OMIM ID: 145260
HumanWNK165125WNK lysine deficient protein kinase 1
img HP RolledUp, OMIM ID: 145260
HumanNSD164324nuclear receptor binding SET domain protein 1
img HP TAS, OMIM ID: 130650
HumanPEX2655670peroxisomal biogenesis factor 26
img HP RolledUp, OMIM ID: 202370
img HP RolledUp, OMIM ID: 214100
HumanCHD755636chromodomain helicase DNA binding protein 7
img HP TAS, OMIM ID: 214800
HumanRBM2855131RNA binding motif protein 28
img HP RolledUp, OMIM ID: 612079
HumanMKS154903Meckel syndrome, type 1
img HP RolledUp, OMIM ID: 249000
HumanMAGEL254551MAGE-like 2
img HP RolledUp, OMIM ID: 176270
HumanWNT454361wingless-type MMTV integration site family, member 4
img HP RolledUp, OMIM ID: 611812
HumanRAB4B53916RAB4B, member RAS oncogene family
img HP RolledUp, OMIM ID: 612945
HumanPDE11A50940phosphodiesterase 11A
img HP RolledUp, OMIM ID: 610475
HumanNSDHL50814NAD(P) dependent steroid dehydrogenase-like
img HP TAS, OMIM ID: 308050
HumanTCTN326123tectonic family member 3
img HP RolledUp, OMIM ID: 258860
HumanNPAP123742nuclear pore associated protein 1
img HP RolledUp, OMIM ID: 176270
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000834Abnormality of the adrenal glands0self