| D011038 |
Rothmund-Thomson Syndrome |
An autosomal recessive syndrome occurring principally in females, characterized by the presence of reticulated, atrophic, hyperpigmented, telangiectatic cutaneous plaques, often accompanied by juvenile cataracts, saddle nose, congenital bone defects, disturbances in the growth of HAIR; NAILS; and TEETH; and HYPOGONADISM. |
Poikiloderma Congenitale,Congenital Poikiloderma,Poikiloderma Atrophicans and Cataract,Poikiloderma Congenitale of Rothmund-Thomson,Poikiloderma of Rothmund-Thomson,Congenitale, Poikiloderma,Congenitales, Poikiloderma,Poikiloderma Congenitales,Poikiloderma of Rothmund Thomson,Rothmund Thomson Syndrome,Rothmund-Thomson Poikiloderma,Rothmund-Thomson Poikilodermas,Syndrome, Rothmund-Thomson |
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| D005260 |
Female |
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Females |
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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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| D012867 |
Skin |
The outer covering of the body that protects it from the environment. It is composed of the DERMIS and the EPIDERMIS. |
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| D012871 |
Skin Diseases |
Diseases involving the DERMIS or EPIDERMIS. |
Dermatoses,Skin and Subcutaneous Tissue Disorders,Dermatosis,Skin Disease |
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