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Stomatognathic Diseases (group results) Stomatognathic Diseases [MESH:D009057] (30) C08. Respiratory Tract Diseases (group results) Respiratory Tract Diseases [MESH:D012140] (29) Z. Exceptions (26) C09. Otorhinolaryngologic Diseases (group results) Otorhinolaryngologic Diseases [MESH:D010038] (29) C10. Nervous System Diseases (group results) Nervous System Diseases [MESH:D009422] (30) Z. Exceptions (29) C11. Eye Diseases (group results) Eye Diseases [MESH:D005128] (29) Z. Exceptions (8) C12. Male Urogenital Diseases (group results) Male Urogenital Diseases [MESH:D052801] (29) C13. Female Urogenital Diseases and Pregnancy Complications (group results) Female Urogenital Diseases [MESH:D052776] (29) Pregnancy Complications [MESH:D011248] (29) Z. Exceptions (27) C14. Cardiovascular Diseases (group results) Cardiovascular Diseases [MESH:D002318] (30) Z. Exceptions (29) C15. Hemic and Lymphatic Diseases (group results) Hematologic Diseases [MESH:D006402] (29) Lymphatic Diseases [MESH:D008206] (29) Z. Exceptions (19) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: all > Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Skin Abnormalities [MESH:D012868] > Rothmund-Thomson Syndrome [MESH:D011038] Navajo poikiloderma [MESH:C538345] (1) PARC syndrome [MESH:C537174] (1) Rapadilino syndrome [MESH:C535288] (30) Skeletal Dysplasia with Telangiectases and Mesodermal Dysgenesis of the Iris [MESH:C564819] (1) Spastic paraplegia neuropathy poikiloderma [MESH:C536870] (1) C17. Skin and Connective Tissue Diseases (group results) Connective Tissue Diseases [MESH:D003240] (29) Skin Diseases [MESH:D012871] (35) C18. Nutritional and Metabolic Diseases (group results) Metabolic Diseases [MESH:D008659] (35) Nutrition Disorders [MESH:D009748] (29) Z. Exceptions (22) C19. Endocrine System Diseases (group results) Endocrine System Diseases [MESH:D004700] (30) Z. Exceptions (10) C20. Immune System Diseases (group results) Immune System Diseases [MESH:D007154] (29) Z. Exceptions (13) C21. Disorders of Environmental Origin C22. Animal Diseases (group results) Animal Diseases [MESH:D000820] (29) C23. Pathological Conditions, Signs and Symptoms (group results) Pathologic Processes [MESH:D010335] (29) Pathological Conditions, Anatomical [MESH:D020763] (30) Signs and Symptoms [MESH:D012816] (29) C24. Occupational Diseases (group results) Occupational Diseases [MESH:D009784] (29) Z. Exceptions (28) C25. Chemically-Induced Disorders (group results) Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (29) Poisoning [MESH:D011041] (29) Substance-Related Disorders [MESH:D019966] (29) C26. Wounds and Injuries (group results) Wounds and Injuries [MESH:D014947] (29) Z. Exceptions (28) D01. 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These terms define your current search. Click the × to remove a term. C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Skin Abnormalities [MESH:D012868] > Rothmund-Thomson Syndrome [MESH:D011038] × 35 items, grouped by C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities (view ungrouped items) Navajo poikiloderma [MESH:C538345] (1)    MESH:C538345   Navajo poikiloderma C538345               PARC syndrome [MESH:C537174] (1)    MESH:C537174   PARC syndrome C537174               Rapadilino syndrome [MESH:C535288] (30)    MESH:C015559   trimellitic anhydride C015559               MESH:C016403   2,4-dinitrotoluene C016403               MESH:C023514   2,6-dinitrotoluene C023514               MESH:C025462   sulindac sulfide C025462               MESH:C025589   ochratoxin A C025589               MESH:C029497   2,3-bis(3'-hydroxybenzyl)butyrolactone C029497               MESH:C031927   hydroquinone C031927               MESH:C039281   furan C039281               MESH:C057693   troglitazone C057693               MESH:C059514   resveratrol C059514               MESH:C400082   bortezomib C400082               MESH:C535288   Rapadilino syndrome C535288               MESH:C558013   NSC 689534 C558013               MESH:D000535   Aluminum D000535               MESH:D002117   Calcitriol D002117               MESH:D002509   Cephaloridine D002509               MESH:D002994   Clofibrate D002994               MESH:D003300   Copper D003300               MESH:D003375   Coumestrol D003375               MESH:D004137   Dinitrochlorobenzene D004137               MESH:D004237   Diuron D004237               MESH:D005472   Fluorouracil D005472               MESH:D005944   Glucosamine D005944               MESH:D007854   Lead D007854               MESH:D010081   Oxazolone D010081               MESH:D011794   Quercetin D011794               MESH:D013739   Testosterone D013739               MESH:D013749   Tetrachlorodibenzodioxin D013749               MESH:D014051   Toluene 2,4-Diisocyanate D014051               MESH:D019327   Copper Sulfate D019327               Skeletal Dysplasia with Telangiectases and Mesodermal Dysgenesis of the Iris [MESH:C564819] (1)    MESH:C564819   Skeletal Dysplasia with Telangiectases and Mesodermal Dysgenesis of the Iris C564819               Spastic paraplegia neuropathy poikiloderma [MESH:C536870] (1)    MESH:C536870   Spastic paraplegia neuropathy poikiloderma C536870                (others) (1)    MESH:D011038   Rothmund-Thomson Syndrome D011038