MeSH Treeview
Query OMIM entry list
190320
-
TRICHODENTOOSSEOUS SYNDROME
→
High-scoring List
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Craniofacial Dysostosis
Osteochondrodysplasias
Osteosclerosis
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniofacial Dysostosis
Stomatognathic Diseases
Stomatognathic System Abnormalities
Tooth Abnormalities
Dental Enamel Hypoplasia
Amelogenesis Imperfecta
Dentinogenesis Imperfecta
Tooth Diseases
Tooth Abnormalities
Dental Enamel Hypoplasia
Amelogenesis Imperfecta
Dentinogenesis Imperfecta
Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniofacial Dysostosis
Stomatognathic System Abnormalities
Tooth Abnormalities
Dental Enamel Hypoplasia
Amelogenesis Imperfecta
Dentinogenesis Imperfecta
Genetic Diseases, Inborn
Chromosome Disorders
Eye Diseases, Hereditary
Retinitis Pigmentosa
Skin and Connective Tissue Diseases
Skin Diseases
Hair Diseases
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Disease
Syndrome
Database Center for Life Science