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Pediatric Disease Annotations & Medicines



   mycosis fungoides
  

Disease ID 93
Disease mycosis fungoides
Definition
A chronic, malignant T-cell lymphoma of the skin. In the late stages, the LYMPH NODES and viscera are affected.
Synonym
[m]mycosis fungoides
[m]mycosis fungoides (disorder)
[m]mycosis fungoides nos
[m]mycosis fungoides nos (morphologic abnormality)
ctcl/ mycosis fungoides
cutaneous t-cell lymphoma/mycosis fungoides
granuloma, fungoides
mf - mycosis fungoides
mycosis fungoides (clinical)
mycosis fungoides (disorder)
mycosis fungoides (morphologic abnormality)
mycosis fungoides [disease/finding]
mycosis fungoides lymphoma
mycosis fungoides nos
mycosis fungoides nos (disorder)
mycosis fungoides of unspecified site
mycosis fungoides of unspecified site (disorder)
OMIM
DOID
UMLS
C0026948
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:42)
C0002173  |  follicular mucinosis  |  5
C0024299  |  lymphoma  |  4
C0162855  |  mucinosis  |  4
C1276146  |  cutaneous lymphoma  |  2
C0002726  |  amyloidosis  |  2
C0206180  |  anaplastic large-cell lymphoma  |  1
C0037274  |  dermatosis  |  1
C0024299  |  lymphomas  |  1
C0024314  |  lymphoproliferative disorders  |  1
C0017661  |  iga nephropathy  |  1
C0037998  |  splenic infarction  |  1
C0002170  |  alopecia  |  1
C0206141  |  hypereosinophilic syndrome  |  1
C0042373  |  vascular disease  |  1
C0000889  |  acanthosis nigricans  |  1
C0409974  |  lupus erythematosus  |  1
C0334254  |  lymphoepithelioma  |  1
C0024305  |  non-hodgkin lymphoma  |  1
C0030805  |  bullous pemphigoid  |  1
C0033860  |  psoriasis  |  1
C0520679  |  obstructive sleep apnea  |  1
C0024314  |  lymphoproliferative disorder  |  1
C0268397  |  cutaneous amyloidosis  |  1
C0024141  |  systemic lupus erythematosus  |  1
C0016436  |  folliculitis  |  1
C0039590  |  testicular cancer  |  1
C1332362  |  b-cell neoplasm  |  1
C0023448  |  lymphocytic leukaemia  |  1
C0020437  |  hypercalcemia  |  1
C0011603  |  dermatitis  |  1
C0036920  |  sezary syndrome  |  1
C1302772  |  primary cutaneous lymphoma  |  1
C0023434  |  chronic lymphocytic leukaemia  |  1
C0007222  |  cardiovascular disease  |  1
C0079773  |  cutaneous t-cell lymphoma  |  1
C0019829  |  hodgkin lymphoma  |  1
C0037315  |  sleep apnea  |  1
C0022658  |  nephropathy  |  1
C0023348  |  lepromatous leprosy  |  1
C0152965  |  staphylococcal sepsis  |  1
C0042109  |  urticarial  |  1
C0021843  |  bowel obstruction  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
TNFRSF1B  |  7133  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:206)
6362  |  CCL18  |  DISEASES
10344  |  CCL26  |  DISEASES
933  |  CD22  |  DISEASES
3385  |  ICAM3  |  DISEASES
9319  |  TRIP13  |  DISEASES
30009  |  TBX21  |  DISEASES
3002  |  GZMB  |  DISEASES
6367  |  CCL22  |  DISEASES
6361  |  CCL17  |  DISEASES
973  |  CD79A  |  DISEASES
4818  |  NKG7  |  DISEASES
3558  |  IL2  |  DISEASES
55801  |  IL26  |  DISEASES
3458  |  IFNG  |  DISEASES
4172  |  MCM3  |  DISEASES
4188  |  MDFI  |  DISEASES
3565  |  IL4  |  DISEASES
3567  |  IL5  |  DISEASES
604  |  BCL6  |  DISEASES
5948  |  RBP2  |  DISEASES
11126  |  CD160  |  DISEASES
6402  |  SELL  |  DISEASES
3070  |  HELLS  |  DISEASES
4360  |  MRC1  |  DISEASES
79441  |  HAUS3  |  DISEASES
5335  |  PLCG1  |  DISEASES
10893  |  MMP24  |  DISEASES
1236  |  CCR7  |  DISEASES
10875  |  FGL2  |  DISEASES
968  |  CD68  |  DISEASES
1036  |  CDO1  |  DISEASES
79977  |  GRHL2  |  DISEASES
83483  |  PLVAP  |  DISEASES
3727  |  JUND  |  DISEASES
10752  |  CHL1  |  DISEASES
29969  |  MDFIC  |  DISEASES
4836  |  NMT1  |  DISEASES
6366  |  CCL21  |  DISEASES
10850  |  CCL27  |  DISEASES
9099  |  USP2  |  DISEASES
10113  |  PREB  |  DISEASES
5862  |  RAB2A  |  DISEASES
5264  |  PHYH  |  DISEASES
3682  |  ITGAE  |  DISEASES
3574  |  IL7  |  DISEASES
10578  |  GNLY  |  DISEASES
943  |  TNFRSF8  |  DISEASES
867  |  CBL  |  DISEASES
10382  |  TUBB4A  |  DISEASES
6774  |  STAT3  |  DISEASES
3383  |  ICAM1  |  DISEASES
27074  |  LAMP3  |  DISEASES
7112  |  TMPO  |  DISEASES
54509  |  RHOF  |  DISEASES
7157  |  TP53  |  DISEASES
1939  |  EIF2D  |  DISEASES
2052  |  EPHX1  |  DISEASES
9180  |  OSMR  |  DISEASES
3001  |  GZMA  |  DISEASES
1030  |  CDKN2B  |  DISEASES
3439  |  IFNA1  |  DISEASES
7424  |  VEGFC  |  DISEASES
4154  |  MBNL1  |  DISEASES
3672  |  ITGA1  |  DISEASES
925  |  CD8A  |  DISEASES
7070  |  THY1  |  DISEASES
7345  |  UCHL1  |  DISEASES
7508  |  XPC  |  DISEASES
9337  |  CNOT8  |  DISEASES
10563  |  CXCL13  |  DISEASES
9372  |  ZFYVE9  |  DISEASES
9437  |  NCR1  |  DISEASES
1234  |  CCR5  |  DISEASES
6777  |  STAT5B  |  DISEASES
10630  |  PDPN  |  DISEASES
7412  |  VCAM1  |  DISEASES
2215  |  FCGR3B  |  DISEASES
3577  |  CXCR1  |  DISEASES
3600  |  IL15  |  DISEASES
9265  |  CYTH3  |  DISEASES
10922  |  FASTK  |  DISEASES
10206  |  TRIM13  |  DISEASES
94235  |  GNG8  |  DISEASES
353514  |  LILRA5  |  DISEASES
3603  |  IL16  |  DISEASES
3689  |  ITGB2  |  DISEASES
3688  |  ITGB1  |  DISEASES
121355  |  GTSF1  |  DISEASES
171558  |  PTCRA  |  DISEASES
3596  |  IL13  |  DISEASES
3627  |  CXCL10  |  DISEASES
6373  |  CXCL11  |  DISEASES
27087  |  B3GAT1  |  DISEASES
8763  |  CD164  |  DISEASES
947  |  CD34  |  DISEASES
924  |  CD7  |  DISEASES
666  |  BOK  |  DISEASES
1191  |  CLU  |  DISEASES
6047  |  RNF4  |  DISEASES
30835  |  CD209  |  DISEASES
6773  |  STAT2  |  DISEASES
57381  |  RHOJ  |  DISEASES
4684  |  NCAM1  |  DISEASES
29851  |  ICOS  |  DISEASES
10938  |  EHD1  |  DISEASES
9235  |  IL32  |  DISEASES
3812  |  KIR3DL2  |  DISEASES
64332  |  NFKBIZ  |  DISEASES
1237  |  CCR8  |  DISEASES
6401  |  SELE  |  DISEASES
3838  |  KPNA2  |  DISEASES
5133  |  PDCD1  |  DISEASES
9094  |  UNC119  |  DISEASES
112744  |  IL17F  |  DISEASES
8631  |  SKAP1  |  DISEASES
23583  |  SMUG1  |  DISEASES
7060  |  THBS4  |  DISEASES
6776  |  STAT5A  |  DISEASES
54345  |  SOX18  |  DISEASES
921  |  CD5  |  DISEASES
56940  |  DUSP22  |  DISEASES
80705  |  TSGA10  |  DISEASES
355  |  FAS  |  DISEASES
5358  |  PLS3  |  DISEASES
140885  |  SIRPA  |  DISEASES
3683  |  ITGAL  |  DISEASES
64919  |  BCL11B  |  DISEASES
5079  |  PAX5  |  DISEASES
26052  |  DNM3  |  DISEASES
6775  |  STAT4  |  DISEASES
2526  |  FUT4  |  DISEASES
9332  |  CD163  |  DISEASES
7037  |  TFRC  |  DISEASES
6693  |  SPN  |  DISEASES
170482  |  CLEC4C  |  DISEASES
4311  |  MME  |  DISEASES
1803  |  DPP4  |  DISEASES
9760  |  TOX  |  DISEASES
4283  |  CXCL9  |  DISEASES
80342  |  TRAF3IP3  |  DISEASES
1380  |  CR2  |  DISEASES
5788  |  PTPRC  |  DISEASES
51696  |  HECA  |  DISEASES
2214  |  FCGR3A  |  DISEASES
51744  |  CD244  |  DISEASES
115352  |  FCRL3  |  DISEASES
6278  |  S100A7  |  DISEASES
6280  |  S100A9  |  DISEASES
4942  |  OAT  |  DISEASES
5406  |  PNLIP  |  DISEASES
914  |  CD2  |  DISEASES
6847  |  SYCP1  |  DISEASES
959  |  CD40LG  |  DISEASES
1791  |  DNTT  |  DISEASES
51213  |  LUZP4  |  DISEASES
2833  |  CXCR3  |  DISEASES
3561  |  IL2RG  |  DISEASES
1043  |  CD52  |  DISEASES
6257  |  RXRB  |  DISEASES
50943  |  FOXP3  |  DISEASES
7133  |  TNFRSF1B  |  DISEASES
548313  |  SSX4B  |  DISEASES
6759  |  SSX4  |  DISEASES
386653  |  IL31  |  DISEASES
4609  |  MYC  |  DISEASES
10497  |  UNC13B  |  DISEASES
7293  |  TNFRSF4  |  DISEASES
2625  |  GATA3  |  DISEASES
3559  |  IL2RA  |  DISEASES
4507  |  MTAP  |  DISEASES
3440  |  IFNA2  |  DISEASES
3662  |  IRF4  |  DISEASES
51378  |  ANGPT4  |  DISEASES
6624  |  FSCN1  |  DISEASES
238  |  ALK  |  DISEASES
3811  |  KIR3DL1  |  DISEASES
9349  |  RPL23  |  DISEASES
56666  |  PANX2  |  DISEASES
3676  |  ITGA4  |  DISEASES
7110  |  TMF1  |  DISEASES
50489  |  CD207  |  DISEASES
3718  |  JAK3  |  DISEASES
1029  |  CDKN2A  |  DISEASES
147920  |  IGFL2  |  DISEASES
7124  |  TNF  |  DISEASES
6304  |  SATB1  |  DISEASES
7072  |  TIA1  |  DISEASES
54900  |  LAX1  |  DISEASES
3586  |  IL10  |  DISEASES
338376  |  IFNE  |  DISEASES
5793  |  PTPRG  |  DISEASES
30816  |  ERVW-1  |  DISEASES
2533  |  FYB  |  DISEASES
930  |  CD19  |  DISEASES
387357  |  THEMIS  |  DISEASES
488  |  ATP2A2  |  DISEASES
7694  |  ZNF135  |  DISEASES
1232  |  CCR3  |  DISEASES
3684  |  ITGAM  |  DISEASES
605  |  BCL7A  |  DISEASES
89795  |  NAV3  |  DISEASES
567  |  B2M  |  DISEASES
85316  |  BAGE5  |  DISEASES
100302740  |  FAS-AS1  |  DISEASES
407975  |  MIR17HG  |  DISEASES
26801  |  SNORD48  |  DISEASES
Locus(Waiting for update.)
Disease ID 93
Disease mycosis fungoides
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:7)
HP:0002665  |  Lymphoma
HP:0008069  |  Neoplasm of the skin
HP:0000964  |  Eczema
HP:0000989  |  pruritis
HP:0200035  |  Skin plaque
HP:0010783  |  Erythema
HP:0002716  |  Lymph node hyperplasia
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:25)
HP:0002665  |  Lymphoma  |  4
HP:0012190  |  T cell lymphoma  |  3
HP:0001596  |  Hair loss  |  2
HP:0011034  |  Amyloid disease  |  2
HP:0002664  |  Neoplasia  |  2
HP:0002870  |  Obstructive sleep apnea  |  1
HP:0002721  |  Immunodeficiency  |  1
HP:0010535  |  Sleep apnea  |  1
HP:0010783  |  Erythema  |  1
HP:0002725  |  Systemic lupus erythematosus  |  1
HP:0012189  |  Hodgkin disease  |  1
HP:0005214  |  Bowel obstruction  |  1
HP:0005523  |  Lymphoproliferative disorder  |  1
HP:0012192  |  Cutaneous T-cell lymphoma  |  1
HP:0012193  |  Anaplastic large-cell lymphoma  |  1
HP:0000956  |  Keratosis nigricans  |  1
HP:0003765  |  Psoriasis  |  1
HP:0002835  |  Aspiration  |  1
HP:0012539  |  Non-Hodgkin lymphoma  |  1
HP:0000112  |  Nephropathy  |  1
HP:0012309  |  Cutaneous amyloidosis  |  1
HP:0030731  |  Carcinoma  |  1
HP:0001880  |  Eosinophilia  |  1
HP:0000966  |  Decreased sweating  |  1
HP:0003072  |  Hypercalcemia  |  1
Disease ID 93
Disease mycosis fungoides
Manually Symptom
UMLS  | Name(Total Manually Symptoms:77)
C2717981  |  poromas
C2697310  |  sarcoidosis
C2240374  |  eosinophilia
C2116082  |  thyroid nodule
C1963254  |  tumor lysis syndrome
C1963139  |  hypopigmentation
C1565489  |  renal insufficiency
C1373218  |  immunosuppression
C1368404  |  hypopharyngeal carcinoma
C1367970  |  pagetoid reticulosis
C1336753  |  lymphoma of the thyroid gland
C1333177  |  lymphoproliferative disorder of the skin
C1000483  |  anemia
C0936250  |  eczema herpeticum
C0920350  |  hashimoto thyroiditis
C0870082  |  hyperkeratosis
C0748159  |  pulmonary involvement
C0545080  |  composite lymphoma
C0497156  |  lymphadenopathy
C0475858  |  generalized pruritus
C0442874  |  neuropathy
C0403766  |  phimosis
C0272398  |  dermatopathic lymphadenopathy
C0271683  |  motor polyneuropathy
C0268749  |  immunotactoid glomerulopathy
C0268397  |  cutaneous amyloidosis
C0263396  |  pigmented purpuric eruption
C0238790  |  bone destruction
C0238419  |  fournier's gangrene
C0235896  |  lung infiltration
C0221348  |  yellow nail syndrome
C0221207  |  cold urticaria
C0206744  |  idiopathic cd4+ t lymphocytopenia
C0206182  |  lymphomatoid papulosis
C0162855  |  mucinosis
C0155365  |  disorder of vitreous
C0150988  |  sclerodactyly
C0085636  |  light sensitivity
C0079772  |  t-cell lymphomas
C0051981  |  leprosy
C0043325  |  xanthomatosis
C0042338  |  herpes zoster
C0037926  |  spinal cord compression
C0037299  |  skin ulcers
C0037285  |  skin manifestation
C0037284  |  skin lesions
C0031117  |  peripheral neuropathy
C0029166  |  oral manifestations
C0027697  |  nephritis
C0025202  |  malignant melanoma
C0024958  |  maxillary sinus tumor
C0024299  |  lymphomas
C0024299  |  lymphoma
C0022660  |  acute renal failure
C0022603  |  seborrheic keratosis
C0022568  |  keratitis
C0022504  |  kaposi's varicelliform eruption
C0022354  |  obstructive jaundice
C0021843  |  intestinal obstruction
C0021051  |  immunologic deficiency syndromes
C0020598  |  hypocalcemia
C0020097  |  htlv-i infection
C0020097  |  htlv-i
C0019829  |  hodgkin's lymphoma
C0019829  |  hodgkin's disease
C0019829  |  hodgkin lymphoma
C0019372  |  herpes infection
C0010043  |  ulcerative keratitis
C0008489  |  chorea
C0007137  |  squamous cell carcinomas
C0007117  |  basal cell carcinomas
C0003864  |  arthritis
C0002880  |  autoimmune hemolytic anemia
C0002514  |  hyperaminoaciduria
C0002173  |  follicular mucinosis
C0002173  |  alopecia mucinosa
C0000889  |  acanthosis nigricans
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:12)
C0002173  |  follicular mucinosis  |  5
C0162855  |  mucinosis  |  4
C0024299  |  lymphoma  |  4
C0206182  |  lymphomatoid papulosis  |  2
C0014457  |  eosinophilia  |  1
C0019829  |  hodgkin lymphoma  |  1
C0037284  |  skin lesions  |  1
C0024299  |  lymphomas  |  1
C1367970  |  pagetoid reticulosis  |  1
C1333177  |  lymphoproliferative disorder of the skin  |  1
C0000889  |  acanthosis nigricans  |  1
C0268397  |  cutaneous amyloidosis  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:6)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1042522171073937157TP53umls:C0026948BeFreeAssociation of p53 Arg72Pro polymorphism and beta-catenin accumulation in mycosis fungoides.0.0019000932006TP53177676154GT,C
rs1124454412120937864061TSPYL2umls:C0026948BeFreeOne mycosis fungoides and one pleomorphic CTCL harbored a KRAS(G13D) mutation; one Sézary syndrome and one CD30(+) CTCL harbored a NRAS(Q61K) amino acid change.0.0008143262011KRAS1225245347CA,G,T
rs11540654171073937157TP53umls:C0026948BeFreeAssociation of p53 Arg72Pro polymorphism and beta-catenin accumulation in mycosis fungoides.0.0019000932006TP53177676040CT,G,A
rs1214345962120937864061TSPYL2umls:C0026948BeFreeOne mycosis fungoides and one pleomorphic CTCL harbored a KRAS(G13D) mutation; one Sézary syndrome and one CD30(+) CTCL harbored a NRAS(Q61K) amino acid change.0.0008143262011NRAS1114716123CT,G,A
rs1219132382120937864061TSPYL2umls:C0026948BeFreeOne mycosis fungoides and one pleomorphic CTCL harbored a KRAS(G13D) mutation; one Sézary syndrome and one CD30(+) CTCL harbored a NRAS(Q61K) amino acid change.0.0008143262011KRAS1225227343GT,C
rs1219132542120937864061TSPYL2umls:C0026948BeFreeOne mycosis fungoides and one pleomorphic CTCL harbored a KRAS(G13D) mutation; one Sézary syndrome and one CD30(+) CTCL harbored a NRAS(Q61K) amino acid change.0.0008143262011NRAS1114713909GT,C
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0001890Autoimmune hemolytic anemiaMP:0001577anemia;HP:0012189Hodgkin lymphoma
Mapped by homologous gene(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0002716LymphadenopathyMP:0002420abnormal adaptive immunity;HP:0001890Autoimmune hemolytic anemia
Chemical(Total Drugs:4)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0026948arsenic trioxideC0066321327-53-3mycosis fungoidesMESH:D009182therapeutic18349030
C0026948carmustineD002330154-93-8mycosis fungoidesMESH:D009182therapeutic16631939
C0026948methoxsalenD008730298-81-7mycosis fungoidesMESH:D009182therapeutic16259964
C0026948vincristineD014750-mycosis fungoidesMESH:D009182therapeutic1850399
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)