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Details
Link-It Detail - Human Phenotype - Abnormality of the anterior pituitary
Debug Stats
  • ### Total Build Time: 24 ms 26.155 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 212 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 271 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=2 ms Completed: 2 ms rowSize= 467 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 2.056 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.182 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 20.814 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.031 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the anterior pituitary HP:0011747
Definition (1)
An abnormality of the `adenohypophysis` (FMA:74627), which is also known as the anterior lobe of the pituitary gland.
Parents (1)
img Abnormality of the hypothalamus-pituitary axis HP:0000864
Children (6)
img Anterior hypopituitarism HP:0000830
img Pituitary resistance to thyroid hormone HP:0008227
img Anterior pituitary dysgenesis HP:0010625
img Hyperpituitarism HP:0010514
img Neoplasm of the anterior pituitary HP:0011750
img Pituitary calcification HP:0010513
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the hypothalamus-pituitary axis HP:0000864
Genes (105)

Species:
human : 105
Page Size
Current 25
  Page 1 of 5
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDUPXQ27.3Q28100874533
HumanMYMY4100653379Moyamoya disease 4
img HP RolledUp, OMIM ID: 300845
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP RolledUp, OMIM ID: 606407
HumanDEL18Q100216483Chromosome 18q deletion syndrome
img HP RolledUp, OMIM ID: 601808
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
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 RolledUp, OMIM ID: 180860
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
img HP RolledUp, OMIM ID: 216550
HumanLIPI149998lipase, member I
HumanPWAR1145624Prader Willi/Angelman region RNA 1
img HP RolledUp, OMIM ID: 176270
HumanB3GALTL145173beta 1,3-galactosyltransferase-like
img HP RolledUp, OMIM ID: 261540
HumanRSS140821Russell Silver syndrome
img HP RolledUp, OMIM ID: 180860
HumanAPOA5116519apolipoprotein A-V
HumanLHX489884LIM homeobox 4
img HP RolledUp, OMIM ID: 262700
HumanDCAF1780067DDB1 and CUL4 associated factor 17
HumanSECISBP279048SECIS binding protein 2
img HP RolledUp, OMIM ID: 609698
HumanHTGS56797Hypertriglyceridemia, familial
HumanCHD755636chromodomain helicase DNA binding protein 7
img HP RolledUp, OMIM ID: 214800
HumanSLC29A355315solute carrier family 29 (equilibrative nucleoside transporter), member 3
img HP RolledUp, OMIM ID: 612391
img HP RolledUp, OMIM ID: 602782
HumanMAGEL254551MAGE-like 2
img HP RolledUp, OMIM ID: 176270
HumanSMARCAL150485SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
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:0011747Abnormality of the anterior pituitary0self