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Pediatric Disease Annotations & Medicines



   chronic recurrent multifocal osteomyelitis
  

Disease ID 572
Disease chronic recurrent multifocal osteomyelitis
Definition
An autoinflammatory disease characterized by sterile bone lesions which are multifocal and/or recurrent.
Synonym
chronic multifocal osteomyelitis
chronic multifocal osteomyelitis (disorder)
cmo
crmo
crmo - chronic multifocal osteomyelitis
multifocal osteomyelitis, chronic
nbo
non-bacterial osteomyelitis
osteomyelitis, chronic multifocal
Orphanet
OMIM
UMLS
C0410422
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:5)
C0020492  |  hyperostosis  |  1
C0009324  |  ulcerative colitis  |  1
C0010346  |  crohn's disease  |  1
C0006663  |  calcinosis  |  1
C0034212  |  pyoderma  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:60)
7414  |  VCL  |  DISEASES
5411  |  PNN  |  DISEASES
54  |  ACP5  |  DISEASES
4210  |  MEFV  |  DISEASES
1445  |  CSK  |  DISEASES
3381  |  IBSP  |  DISEASES
55907  |  CMAS  |  DISEASES
3554  |  IL1R1  |  DISEASES
79977  |  GRHL2  |  DISEASES
10912  |  GADD45G  |  DISEASES
1401  |  CRP  |  DISEASES
3569  |  IL6  |  DISEASES
3557  |  IL1RN  |  DISEASES
26525  |  IL36RN  |  DISEASES
9663  |  LPIN2  |  DISEASES
3553  |  IL1B  |  DISEASES
1820  |  ARID3A  |  DISEASES
2252  |  FGF7  |  DISEASES
53942  |  CNTN5  |  DISEASES
22934  |  RPIA  |  DISEASES
6352  |  CCL5  |  DISEASES
2487  |  FRZB  |  DISEASES
5896  |  RAG1  |  DISEASES
56246  |  MRAP  |  DISEASES
197259  |  MLKL  |  DISEASES
2147  |  F2  |  DISEASES
1375  |  CPT1B  |  DISEASES
7172  |  TPMT  |  DISEASES
5745  |  PTH1R  |  DISEASES
796  |  CALCA  |  DISEASES
114548  |  NLRP3  |  DISEASES
5313  |  PKLR  |  DISEASES
29949  |  IL19  |  DISEASES
5789  |  PTPRD  |  DISEASES
1822  |  ATN1  |  DISEASES
23556  |  PIGN  |  DISEASES
841  |  CASP8  |  DISEASES
6772  |  STAT1  |  DISEASES
4514  |  MT-CO3  |  DISEASES
3459  |  IFNGR1  |  DISEASES
6708  |  SPTA1  |  DISEASES
632  |  BGLAP  |  DISEASES
262  |  AMD1  |  DISEASES
249  |  ALPL  |  DISEASES
7133  |  TNFRSF1B  |  DISEASES
5251  |  PHEX  |  DISEASES
2591  |  GALNT3  |  DISEASES
57614  |  KIAA1468  |  DISEASES
644150  |  WIPF3  |  DISEASES
57703  |  CWC22  |  DISEASES
9050  |  PSTPIP2  |  DISEASES
7124  |  TNF  |  DISEASES
834  |  CASP1  |  DISEASES
3586  |  IL10  |  DISEASES
54751  |  FBLIM1  |  DISEASES
6452  |  SH3BP2  |  DISEASES
284  |  ANGPT1  |  DISEASES
8972  |  MGAM  |  DISEASES
9051  |  PSTPIP1  |  DISEASES
79104  |  MEG8  |  DISEASES
Locus(Waiting for update.)
Disease ID 572
Disease chronic recurrent multifocal osteomyelitis
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:29)
HP:0002037  |  Inflammation of the large intestine
HP:0100847  |  Palmoplantar pustulosis
HP:0001824  |  Weight loss
HP:0000988  |  Skin rash
HP:0002797  |  Osteolysis
HP:0011227  |  Elevated C-reactive protein level
HP:0005930  |  Abnormality of epiphysis morphology
HP:0001945  |  Fever
HP:0001939  |  Laboratory abnormality
HP:0004396  |  Poor appetite
HP:0005901  |  Chronic recurrent multifocal osteomyelitis
HP:0000969  |  Edema
HP:0100774  |  Hyperostosis
HP:0000989  |  Pruritus
HP:0012378  |  Fatigue
HP:0002633  |  Vasculitis
HP:0001061  |  Acne
HP:0001369  |  Arthritis
HP:0005464  |  Craniofacial osteosclerosis
HP:0100781  |  Abnormality of the sacroiliac joint
HP:0003765  |  Psoriasis
HP:0006824  |  Cranial nerve paralysis
HP:0001903  |  Anemia
HP:0002650  |  Scoliosis
HP:0002653  |  Bone pain
HP:0000944  |  Abnormality of the metaphyses
HP:0003468  |  Abnormality of the vertebrae
HP:0003565  |  Elevated erythrocyte sedimentation rate
HP:0002754  |  Osteomyelitis
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:6)
HP:0001945  |  Fever  |  2
HP:0100280  |  Morbus Crohn  |  1
HP:0000999  |  Pyoderma  |  1
HP:0003761  |  Calcinosis  |  1
HP:0100774  |  Hyperostosis  |  1
HP:0100279  |  Ulcerative colitis  |  1
Disease ID 572
Disease chronic recurrent multifocal osteomyelitis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:1)
C0029408  |  degenerative arthritis
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
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:0011001Increased bone mineral densityMP:0000107abnormal frontal bone morphology;HP:0004370Abnormality of temperature regulation
Mapped by homologous gene(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0002633VasculitisMP:0002498abnormal acute inflammation;HP:0002754Osteomyelitis
Chemical(Total Drugs:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)