| UMLS CUI |
UMLS Term |
Proteins |
|
C0002382
|
Alveolar Bone Loss
|
ALPL,
TNFSF11
|
|
C0002452
|
Amelogenesis Imperfecta
|
FAM83H,
LTBP3
|
|
C0004779
|
Basal Cell Nevus Syndrome
|
GLI2,
SUFU,
PTCH1
|
|
C0004943
|
Behcet Syndrome
|
HLA-B,
APOA1,
APOB,
ICAM1,
CXCL8,
IL10,
IL12A,
ITGB2,
SERPINE1,
ERAP1,
TLR4,
C4A,
KLRC4
|
|
C0008924
|
Cleft Lip
|
SPRY2,
MTHFS,
FGF2,
FGF7,
FGF9,
FGFR1,
FGFR2,
IRF6,
MTHFR,
MTR,
MYC,
NOS3,
PTCH1,
SLC19A1,
TYMS,
MAFB
|
|
C0008925
|
Cleft Palate
|
SPRY2,
MTHFS,
DLG1,
FGF2,
FGF7,
FGF9,
FGFR1,
FGFR2,
IRF6,
MNT,
MTR,
MYC,
NOS3,
PDGFRA,
BNC2,
PTCH1,
SIM2,
SLC19A1,
TGFB1,
TGFB2,
TYMS,
FZD4,
CASK,
CBFB
|
|
C0011334
|
Dental Caries
|
CDKN3,
RPS6KA2
|
|
C0011436
|
Dentinogenesis Imperfecta
|
DSPP
|
|
C0014518
|
Toxic Epidermal Necrolysis
|
HLA-B
|
|
C0015469
|
Facial Paralysis
|
POMC
|
|
C0017566
|
Gingival Hyperplasia
|
FGF7,
PDGFB
|
|
C0017567
|
Gingival Hypertrophy
|
ANTXR2
|
|
C0022360
|
Jaw Abnormalities
|
OTX2,
PCSK5,
POLD1
|
|
C0023532
|
Leukoplakia, Oral
|
PTGS2
|
|
C0024433
|
Macrostomia
|
FRAS1
|
|
C0024689
|
Mandibular Diseases
|
MMP2
|
|
C0024950
|
Maxillary Diseases
|
MMP2
|
|
C0026633
|
Mouth Abnormalities
|
PCSK5
|
|
C0026636
|
Mouth Diseases
|
CHAF1A,
FANCG,
DNAJA1,
HSPA14,
DDIT4,
CYP26B1,
PTGS2,
BRCA1,
CHAF1B,
GDF15
|
|
C0026640
|
Mouth Neoplasms
|
NDRG1,
RACK1,
ADH1B,
ADH7,
CRYAB,
CYP1B1,
DSPP,
ENO1,
FGA,
GAPDH,
SFN,
ANXA1,
ANXA2,
ANXA5,
HOXD10,
HSPB1,
ICAM1,
IL18,
KRAS,
LGALS7,
PGAM1,
PIK3CA,
PPIA,
PRTFDC1,
PTGS2,
SERPINB3,
SOD2,
TP53,
TPI1,
TSC2,
UMPS,
VDAC2
|
|
C0027439
|
Nasopharyngeal Neoplasms
|
WIF1,
CYP2A6,
EDNRA,
EGFR,
MMP2,
TNFRSF19
|
|
C0029172
|
Oral Submucous Fibrosis
|
MICA,
COL1A1,
COL1A2,
CST3,
FGF2,
LOX,
MMP1,
MMP2,
MMP9,
PTGS2,
TGFB1,
TIMP1,
TNF
|
|
C0029295
|
Oropharyngeal Neoplasms
|
NDRG1
|
|
C0031030
|
Periapical Periodontitis
|
FGF2
|
|
C0031090
|
Periodontal Diseases
|
CTSC
|
|
C0031099
|
Periodontitis
|
CRP,
NKAIN2,
BIRC5,
MMP9
|
|
C0031106
|
Periodontitis, Juvenile
|
CTSC
|
|
C0031347
|
Pharyngeal Neoplasms
|
ADH1B,
ADH7
|
|
C0031900
|
Pierre Robin Syndrome
|
SOX9
|
|
C0036095
|
Salivary Gland Neoplasms
|
VCAN,
DAPK1,
JAG1,
FAT1,
RBFOX2,
ASPM,
GAS6,
IGFBP2,
ITGB4,
MARCKS,
ISYNA1,
DTL,
GINS2,
SERPINF1,
BCL11A,
PRKD1,
SLC24A3,
PYGB,
ST3GAL4,
SON,
SOX4,
TOP2A,
WNT5B,
NETO2,
HOMER3,
ESPL1
|
|
C0038325
|
Stevens-Johnson Syndrome
|
IKZF1,
CELF2,
PARP1,
CTNNB1,
EP300,
ALB,
HLA-A,
HLA-B,
HLA-C,
MIF,
NUCB1,
PTGER3,
PTGIS,
RB1,
VCP,
CUL4A,
CAV1,
ELMO1,
RBX1
|
|
C0038362
|
Stomatitis
|
NBN
|
|
C0038368
|
Stomatognathic Diseases
|
FADD
|
|
C0040411
|
Tongue Neoplasms
|
CRYAB,
HSPB1,
AQP3,
PTGS2,
SOD2,
TYMS
|
|
C0040427
|
Tooth Abnormalities
|
FGFR2,
PITX2,
TMCO1,
ANKH,
RUNX2
|
|
C0040460
|
Toothache
|
NPY1R
|
|
C0149745
|
Oral Ulcer
|
EDN1,
LEP
|
|
C0205730
|
Hereditary Opalescent Dentin (Disorder)
|
DSPP
|
|
C0221060
|
Mobius Syndrome
|
PLXND1,
REV3L
|
|
C0243057
|
Stomatognathic System Abnormalities
|
RUNX2
|
|
C0266929
|
Chronic Periodontitis
|
CXCL12,
TNFSF11
|
|
C0333355
|
Inflammatory Disease Of Mucous Membrane
|
IL1B,
IL1RN,
IL10,
MTHFR,
TGFA
|
|
C0399352
|
Developmental Absence Of Tooth
|
LTBP3
|
|
C0399380
|
Dentin Dyspalsia, Shields Type 2
|
DSPP
|
|
C0524948
|
Maxillofacial Abnormalities
|
MTHFR
|
|
C1527284
|
Dental Pulp Stone
|
DSPP
|
|
C1527336
|
Sjogren'S Syndrome
|
IRAK1BP1,
FCGR2A,
GTF2I,
IL12A,
ITSN2,
PHIP,
TNFAIP3,
PTTG1
|
|
C2973527
|
Dentinogenesis Imperfecta Without Osteogenesis Imperfecta
|
DSPP
|