| D008297 |
Male |
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Males |
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| D006801 |
Humans |
Members of the species Homo sapiens. |
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man |
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| D000293 |
Adolescent |
A person 13 to 18 years of age. |
Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths |
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| D014997 |
XYY Karyotype |
Abnormal genetic constitution in males characterized by an extra Y chromosome. |
Karyotype, XYY,Karyotypes, XYY,XYY Karyotypes |
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| D015897 |
Comorbidity |
The presence of co-existing or additional diseases with reference to an initial diagnosis or with reference to the index condition that is the subject of study. Comorbidity may affect the ability of affected individuals to function and also their survival; it may be used as a prognostic indicator for length of hospital stay, cost factors, and outcome or survival. |
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| D020022 |
Genetic Predisposition to Disease |
A latent susceptibility to disease at the genetic level, which may be activated under certain conditions. |
Genetic Predisposition,Genetic Susceptibility,Predisposition, Genetic,Susceptibility, Genetic,Genetic Predispositions,Genetic Susceptibilities,Predispositions, Genetic,Susceptibilities, Genetic |
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| D020817 |
Asperger Syndrome |
A disorder beginning in childhood whose essential features are persistent impairment in reciprocal social communication and social interaction, and restricted, repetitive patterns of behavior, interests, or activities. These symptoms may limit or impair everyday functioning. (From DSM-5) |
Asperger Disease,Asperger Disorder,Asperger's Disease,Asperger's Disorder,Asperger's Syndrome,Asperger Diseases,Asperger Disorders,Asperger's Diseases,Aspergers Disease,Aspergers Disorder,Aspergers Syndrome,Disease, Asperger,Disease, Asperger's,Diseases, Asperger,Diseases, Asperger's,Disorder, Asperger,Disorder, Asperger's,Disorders, Asperger,Syndrome, Asperger,Syndrome, Asperger's |
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