| 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 |