Biomaterial Database

E MARQUARDT

UI	MeSH Term	Description	Entries
D010214	Papillon-Lefevre Disease	Rare, autosomal recessive disorder occurring between the first and fifth years of life. It is characterized by palmoplantar keratoderma with periodontitis followed by the premature shedding of both deciduous and permanent teeth. Mutations in the gene for CATHEPSIN C have been associated with this disease.	Haim-Monk Syndrome,Keratosis Palmoplantar Periodontopathy,Keratosis Palmoplantaris with Periodontopathia,Papillon Lefevre Disease,Papillon-Lefevre Syndrome,Haim Monk Syndrome,Keratosis Palmoplantar Periodontopathies,Palmoplantar Periodontopathies, Keratosis,Papillon Lefevre Syndrome
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D013060	Speech	Communication through a system of conventional vocal symbols.	Public Speaking,Speaking, Public
D013064	Speech Disorders	Acquired or developmental conditions marked by an impaired ability to comprehend or generate spoken forms of language.	Aprosodia,Aprosodic Speech,Cluttering,Dysglossia,Dyslalia,Rhinolalia,Verbal Fluency Disorders,Aprosodias,Clutterings,Dysglossias,Dyslalias,Rhinolalias,Speech, Aprosodic,Verbal Fluency Disorder
D013070	Speech Therapy	Treatment for individuals with speech defects and disorders that involves counseling and use of various exercises and aids to help the development of new speech habits.	Therapy, Speech,Speech Therapies,Therapies, Speech