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PedAM

Pediatric Disease Annotations & Medicines



   hypopituitarism
  

Disease ID 221
Disease hypopituitarism
Definition
Diminution or cessation of secretion of one or more hormones from the anterior pituitary gland (including LH; FOLLICLE STIMULATING HORMONE; SOMATOTROPIN; and CORTICOTROPIN). This may result from surgical or radiation ablation, non-secretory PITUITARY NEOPLASMS, metastatic tumors, infarction, PITUITARY APOPLEXY, infiltrative or granulomatous processes, and other conditions.
Synonym
adenohypophyseal hyposecret
adenohypophyseal hyposecretion
anterior pituitary hyposecret syndrome
anterior pituitary hyposecretion syndrome
deficiencies pituitary
deficient secretion of one or more pituitary hormones
hypopituitarism (disorder)
hypopituitarism [disease/finding]
hypopituitarism nos
hypopituitarism nos (disorder)
hypopituitarism, nos
hypopitutitarism
hyposecret adenohypophyseal
hyposecret syndrome anterior pituitary
hyposecretion syndrome, anterior pituitary
hyposecretion, adenohypophyseal
insufficiency pituitary
insufficiency, pituitary
pituitary deficiency
pituitary failure
pituitary hypofunction
pituitary insufficiency
pituitary insufficiency nos
pituitary insufficiency, nos
Orphanet
DOID
ICD10
UMLS
C0020635
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:54)
C0013338  |  growth hormone deficiency  |  6
C0020676  |  hypothyroidism  |  5
C0011848  |  diabetes insipidus  |  4
C0032000  |  pituitary adenoma  |  4
C0020619  |  hypogonadism  |  4
C0011847  |  diabetes  |  3
C0030312  |  pancytopenia  |  3
C0032000  |  pituitary adenomas  |  3
C0001206  |  acromegaly  |  3
C0242342  |  sheehan's syndrome  |  3
C0878544  |  cardiomyopathy  |  2
C0010276  |  craniopharyngioma  |  2
C0020598  |  hypoglycemia  |  2
C0022735  |  hypogonadotropic hypogonadism  |  2
C0020514  |  hyperprolactinemia  |  2
C0079731  |  b-cell lymphoma  |  2
C0040053  |  thrombosis  |  1
C0687720  |  central diabetes insipidus  |  1
C0948740  |  pituitary hypoplasia  |  1
C0342388  |  acth deficiency  |  1
C0271558  |  pituitary necrosis  |  1
C0376358  |  prostate cancer  |  1
C0014038  |  encephalitis  |  1
C0001430  |  adenoma  |  1
C0854486  |  functioning pituitary adenoma  |  1
C0155307  |  chiasmal syndrome  |  1
C0007115  |  thyroid cancer  |  1
C0024299  |  lymphoma  |  1
C0004903  |  beckwith-wiedemann syndrome  |  1
C0271789  |  tsh deficiency  |  1
C0020255  |  hydrocephalus  |  1
C0242342  |  sheehan syndrome  |  1
C0001403  |  addison's disease  |  1
C0242343  |  panhypopituitarism  |  1
C0029456  |  osteoporosis  |  1
C0242342  |  postpartum pituitary necrosis  |  1
C0001623  |  adrenal insufficiency  |  1
C1565489  |  renal insufficiency  |  1
C1535927  |  charge syndrome  |  1
C0342388  |  adrenocorticotropic hormone deficiency  |  1
C0040147  |  thyroiditis  |  1
C0271623  |  secondary hypogonadism  |  1
C0007115  |  thyroid ca  |  1
C0020635  |  pituitary insufficiency  |  1
C0151740  |  increased intracranial pressure  |  1
C0023448  |  lymphoblastic leukemia  |  1
C0007222  |  cardiovascular disease  |  1
C0042373  |  vascular disease  |  1
C0005940  |  bone disease  |  1
C0032002  |  pituitary disease  |  1
C1333387  |  endocrine syndrome  |  1
C0034012  |  delayed puberty  |  1
C0020617  |  hypoglycaemic coma  |  1
C0023449  |  acute lymphoblastic leukemia  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:11)
CYP19A1  |  1588  |  CTD_human
HESX1  |  8820  |  GHR
POU1F1  |  5449  |  GHR
PRL  |  5617  |  CTD_human
CYP17A1  |  1586  |  CTD_human
GLI2  |  2736  |  GHR
PROP1  |  5626  |  GHR
SOX2  |  6657  |  GHR
LHX4  |  89884  |  GHR
OTX2  |  5015  |  GHR
LHX3  |  8022  |  GHR
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:1)
5626  |  PROP1  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:203)
990  |  CDC6  |  DISEASES
128674  |  PROKR2  |  DISEASES
5020  |  OXT  |  DISEASES
23594  |  ORC6  |  DISEASES
55512  |  SMPD3  |  DISEASES
7038  |  TG  |  DISEASES
268  |  AMH  |  DISEASES
166  |  AES  |  DISEASES
3982  |  LIM2  |  DISEASES
6822  |  SULT2A1  |  DISEASES
5864  |  RAB3A  |  DISEASES
55131  |  RBM28  |  DISEASES
9570  |  GOSR2  |  DISEASES
7126  |  TNFAIP1  |  DISEASES
2798  |  GNRHR  |  DISEASES
26952  |  SMR3A  |  DISEASES
51053  |  GMNN  |  DISEASES
3670  |  ISL1  |  DISEASES
2690  |  GHR  |  DISEASES
9421  |  HAND1  |  DISEASES
338  |  APOB  |  DISEASES
9068  |  ANGPTL1  |  DISEASES
2691  |  GHRH  |  DISEASES
9419  |  CRIPT  |  DISEASES
2693  |  GHSR  |  DISEASES
4189  |  DNAJB9  |  DISEASES
968  |  CD68  |  DISEASES
9459  |  ARHGEF6  |  DISEASES
3630  |  INS  |  DISEASES
1911  |  PHC1  |  DISEASES
2488  |  FSHB  |  DISEASES
1401  |  CRP  |  DISEASES
25914  |  RTTN  |  DISEASES
7252  |  TSHB  |  DISEASES
6927  |  HNF1A  |  DISEASES
6610  |  SMPD2  |  DISEASES
2016  |  EMX1  |  DISEASES
80210  |  ARMC9  |  DISEASES
10643  |  IGF2BP3  |  DISEASES
81873  |  ARPC5L  |  DISEASES
10817  |  FRS3  |  DISEASES
6496  |  SIX3  |  DISEASES
3290  |  HSD11B1  |  DISEASES
79817  |  MOB3B  |  DISEASES
9894  |  TELO2  |  DISEASES
6132  |  RPL8  |  DISEASES
7089  |  TLE2  |  DISEASES
6855  |  SYP  |  DISEASES
10994  |  ILVBL  |  DISEASES
9789  |  SPCS2  |  DISEASES
89884  |  LHX4  |  DISEASES
5000  |  ORC4  |  DISEASES
5443  |  POMC  |  DISEASES
80321  |  CEP70  |  DISEASES
5307  |  PITX1  |  DISEASES
597  |  BCL2A1  |  DISEASES
10733  |  PLK4  |  DISEASES
23432  |  GPR161  |  DISEASES
5972  |  REN  |  DISEASES
1393  |  CRHBP  |  DISEASES
4594  |  MUT  |  DISEASES
3484  |  IGFBP1  |  DISEASES
2796  |  GNRH1  |  DISEASES
1392  |  CRH  |  DISEASES
4863  |  NPAT  |  DISEASES
83439  |  TCF7L1  |  DISEASES
3087  |  HHEX  |  DISEASES
4838  |  NODAL  |  DISEASES
286053  |  NSMCE2  |  DISEASES
6750  |  SST  |  DISEASES
6777  |  STAT5B  |  DISEASES
60675  |  PROK2  |  DISEASES
3549  |  IHH  |  DISEASES
8820  |  HESX1  |  DISEASES
25886  |  POC1A  |  DISEASES
6469  |  SHH  |  DISEASES
83550  |  GPR101  |  DISEASES
915  |  CD3D  |  DISEASES
81620  |  CDT1  |  DISEASES
5617  |  PRL  |  DISEASES
3479  |  IGF1  |  DISEASES
7200  |  TRH  |  DISEASES
1493  |  CTLA4  |  DISEASES
5308  |  PITX2  |  DISEASES
147  |  ADRA1B  |  DISEASES
9079  |  LDB2  |  DISEASES
9915  |  ARNT2  |  DISEASES
64852  |  TUT1  |  DISEASES
695  |  BTK  |  DISEASES
7201  |  TRHR  |  DISEASES
2000  |  ELF4  |  DISEASES
5626  |  PROP1  |  DISEASES
3952  |  LEP  |  DISEASES
2688  |  GH1  |  DISEASES
2771  |  GNAI2  |  DISEASES
51574  |  LARP7  |  DISEASES
4234  |  METTL1  |  DISEASES
1442  |  CSH1  |  DISEASES
2692  |  GHRHR  |  DISEASES
2253  |  FGF8  |  DISEASES
2274  |  FHL2  |  DISEASES
84126  |  ATRIP  |  DISEASES
6657  |  SOX2  |  DISEASES
63925  |  ZNF335  |  DISEASES
10293  |  TRAIP  |  DISEASES
4990  |  SIX6  |  DISEASES
10785  |  WDR4  |  DISEASES
84295  |  PHF6  |  DISEASES
3543  |  IGLL1  |  DISEASES
6906  |  SERPINA7  |  DISEASES
8971  |  H1FX  |  DISEASES
84679  |  SLC9A7  |  DISEASES
83482  |  SCRT1  |  DISEASES
286410  |  ATP11C  |  DISEASES
51738  |  GHRL  |  DISEASES
80254  |  CEP63  |  DISEASES
4221  |  MEN1  |  DISEASES
7225  |  TRPC6  |  DISEASES
7518  |  XRCC4  |  DISEASES
5449  |  POU1F1  |  DISEASES
545  |  ATR  |  DISEASES
55755  |  CDK5RAP2  |  DISEASES
5015  |  OTX2  |  DISEASES
54820  |  NDE1  |  DISEASES
57596  |  BEGAIN  |  DISEASES
26503  |  SLC17A5  |  DISEASES
91687  |  CENPL  |  DISEASES
26052  |  DNM3  |  DISEASES
5116  |  PCNT  |  DISEASES
147409  |  DSG4  |  DISEASES
9782  |  MATR3  |  DISEASES
2736  |  GLI2  |  DISEASES
259230  |  SGMS1  |  DISEASES
23137  |  SMC5  |  DISEASES
24149  |  ZNF318  |  DISEASES
3664  |  IRF6  |  DISEASES
9095  |  TBX19  |  DISEASES
51506  |  UFC1  |  DISEASES
632  |  BGLAP  |  DISEASES
23036  |  ZNF292  |  DISEASES
6566  |  SLC16A1  |  DISEASES
2316  |  FLNA  |  DISEASES
2773  |  GNAI3  |  DISEASES
4791  |  NFKB2  |  DISEASES
6658  |  SOX3  |  DISEASES
959  |  CD40LG  |  DISEASES
3547  |  IGSF1  |  DISEASES
27022  |  FOXD3  |  DISEASES
56889  |  TM9SF3  |  DISEASES
7737  |  RNF113A  |  DISEASES
4998  |  ORC1  |  DISEASES
8022  |  LHX3  |  DISEASES
57169  |  ZNFX1  |  DISEASES
55661  |  DDX27  |  DISEASES
80712  |  ESX1  |  DISEASES
9355  |  LHX2  |  DISEASES
7088  |  TLE1  |  DISEASES
8928  |  FOXH1  |  DISEASES
123872  |  DNAAF1  |  DISEASES
190  |  NR0B1  |  DISEASES
5080  |  PAX6  |  DISEASES
10300  |  KATNB1  |  DISEASES
551  |  AVP  |  DISEASES
6462  |  SHBG  |  DISEASES
54875  |  CNTLN  |  DISEASES
3030  |  HADHA  |  DISEASES
3486  |  IGFBP3  |  DISEASES
6473  |  SHOX  |  DISEASES
55835  |  CENPJ  |  DISEASES
5618  |  PRLR  |  DISEASES
51244  |  CCDC174  |  DISEASES
80757  |  TMEM121  |  DISEASES
1443  |  CSH2  |  DISEASES
174  |  AFP  |  DISEASES
2737  |  GLI3  |  DISEASES
163223  |  ZNF676  |  DISEASES
22995  |  CEP152  |  DISEASES
9718  |  ECE2  |  DISEASES
2492  |  FSHR  |  DISEASES
284403  |  WDR62  |  DISEASES
2641  |  GCG  |  DISEASES
55599  |  RNPC3  |  DISEASES
3481  |  IGF2  |  DISEASES
55636  |  CHD7  |  DISEASES
8861  |  LDB1  |  DISEASES
2260  |  FGFR1  |  DISEASES
8318  |  CDC45  |  DISEASES
8439  |  NSMAF  |  DISEASES
1967  |  EIF2B1  |  DISEASES
3483  |  IGFALS  |  DISEASES
60559  |  SPCS3  |  DISEASES
2675  |  GFRA2  |  DISEASES
137075  |  CLDN23  |  DISEASES
100423062  |  IGLL5  |  DISEASES
9820  |  CUL7  |  DISEASES
27164  |  SALL3  |  DISEASES
246744  |  STH  |  DISEASES
64426  |  SUDS3  |  DISEASES
7090  |  TLE3  |  DISEASES
284424  |  MIR7-3HG  |  DISEASES
100151683  |  RNU4ATAC  |  DISEASES
677833  |  SNORA54  |  DISEASES
692057  |  SNORD12  |  DISEASES
Locus(Waiting for update.)
Disease ID 221
Disease hypopituitarism
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:51)
HP:0000824  |  Growth hormone deficiency  |  6
HP:0000821  |  Underactive thyroid  |  5
HP:0000135  |  Hypogonadism  |  4
HP:0011787  |  Central hypothyroidism  |  4
HP:0000873  |  Diabetes insipidus  |  4
HP:0002893  |  Pituitary adenoma  |  4
HP:0000845  |  Acromegalic growth  |  3
HP:0002664  |  Neoplasia  |  3
HP:0001876  |  Low blood cell count  |  3
HP:0000609  |  Optic nerve hypoplasia  |  3
HP:0001297  |  Cerebral vascular events  |  2
HP:0000870  |  Hyperprolactinemia  |  2
HP:0030062  |  Craniopharyngioma  |  2
HP:0012191  |  B-cell lymphoma  |  2
HP:0001943  |  Hypoglycemia  |  2
HP:0001638  |  Cardiomyopathy  |  2
HP:0011748  |  Adrenocorticotropic hormone deficiency  |  2
HP:0002140  |  Ischemic stroke  |  2
HP:0000938  |  Decreased bone mineral density  |  1
HP:0003510  |  Proportionate dwarfism  |  1
HP:0100842  |  Septo-optic dysplasia  |  1
HP:0000939  |  Osteoporosis  |  1
HP:0008207  |  Addison's disease  |  1
HP:0001259  |  Coma  |  1
HP:0100646  |  Thyroiditis  |  1
HP:0002516  |  Intracranial pressure elevation  |  1
HP:0011734  |  Central adrenal insufficiency  |  1
HP:0002617  |  Aneurysmal dilatation  |  1
HP:0012125  |  Prostate cancer  |  1
HP:0010627  |  Anterior pituitary hypoplasia  |  1
HP:0000871  |  Panhypopituitarism  |  1
HP:0002138  |  Subarachnoid hemorrhage  |  1
HP:0030149  |  Cardiovascular shock  |  1
HP:0012342  |  Macroprolactinoma  |  1
HP:0002383  |  Encephalitis  |  1
HP:0002960  |  Autoimmune condition  |  1
HP:0001325  |  Coma caused by low blood sugar  |  1
HP:0002902  |  Hyponatremia  |  1
HP:0002098  |  Respiratory distress  |  1
HP:0008245  |  Thyroid stimulating hormone deficiency  |  1
HP:0006721  |  Acute lymphocytic leukemia  |  1
HP:0000846  |  Hypoadrenalism  |  1
HP:0000505  |  Poor vision  |  1
HP:0000863  |  Neurohypophyseal diabetes insipidus  |  1
HP:0000083  |  Renal insufficiency  |  1
HP:0000238  |  Nonsyndromal hydrocephalus  |  1
HP:0001508  |  Weight faltering  |  1
HP:0011675  |  Arrhythmias  |  1
HP:0002665  |  Lymphoma  |  1
HP:0005103  |  Calcification of the auricular cartilage  |  1
HP:0000823  |  Pubertal delay  |  1
Disease ID 221
Disease hypopituitarism
Manually Symptom
UMLS  | Name(Total Manually Symptoms:46)
C2697310  |  sarcoidosis
C2364118  |  weakness
C2318511  |  nonalcoholic steatohepatitis
C1963059  |  adrenal insufficiency
C1695689  |  non-dipping
C1555754  |  cardiovascular disease
C1112443  |  male sexual dysfunction
C1000483  |  anemia
C0878544  |  cardiomyopathy
C0856169  |  endothelial dysfunction
C0851302  |  hypoglycemic shock
C0700502  |  primary hypothyroidism
C0600142  |  hot flashes
C0549473  |  thyroid carcinoma
C0497327  |  dementia
C0422833  |  ent symptoms
C0342527  |  androgen deficiency
C0339477  |  lipemia retinalis
C0271801  |  central hypothyroidism
C0271561  |  growth hormone deficiency
C0242339  |  dyslipidemia
C0235394  |  wasting
C0234428  |  disturbances of consciousness
C0233401  |  psychiatric symptom
C0042373  |  vascular disease
C0040156  |  thyrotoxicosis
C0040147  |  thyroiditis
C0033975  |  psychosis
C0032000  |  pituitary adenomas
C0032000  |  pituitary adenoma
C0030421  |  paraganglioma
C0030312  |  pancytopenia
C0020676  |  thyroid insufficiency
C0020625  |  hyponatremia
C0020550  |  hyperthyroidism
C0020473  |  hyperlipidaemia
C0020473  |  hyperlipemia
C0018802  |  congestive heart failure
C0011849  |  diabetes mellitus
C0011608  |  dermatitis herpetiformis
C0009241  |  cognitive disorders
C0004352  |  autism
C0004153  |  atherosclerosis
C0004096  |  asthma
C0002940  |  aneurysm
C0002871  |  anaemia
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:11)
C0271801  |  central hypothyroidism  |  4
C0013338  |  growth hormone deficiency  |  4
C0032000  |  pituitary adenoma  |  3
C0030312  |  pancytopenia  |  3
C0856169  |  endothelial dysfunction  |  2
C0878544  |  cardiomyopathy  |  2
C0042373  |  vascular disease  |  1
C0001623  |  adrenal insufficiency  |  1
C0007115  |  thyroid cancer  |  1
C0007222  |  cardiovascular disease  |  1
C0040147  |  thyroiditis  |  1
Manually Genotype(Total Text Mining Genotypes:0)
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All Snps(Total Genotypes:0)
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GWASdb Annotation(Total Genotypes:0)
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GWASdb Snp Trait(Total Genotypes:0)
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Mapped by lexical matching(Total Items:0)
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Mapped by homologous gene(Total Items:0)
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Chemical(Total Drugs:2)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0020635morphineD00902057-27-2hypopituitarismMESH:D007018marker/mechanism14631063
C0020635progesteroneD01137457-83-0hypopituitarismMESH:D007018therapeutic2673747
FDA approved drug and dosage information(Total Drugs:0)
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FDA labeling changes(Total Drugs:0)
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