<nowiki>Rothmund-Thompson sendromu; ロスムンド・トムソン症候群; syndrome de Rothmund-Thomson; Ротмунд-Томсонов синдром; متلازمة روثموند تومسون; Zespół Rothmunda-Thomsona; Sindrome di Rothmund-Thomson; 로트문드-톰슨 증후군; Синдром Ротмунда–Томсона; Rotmund-Tomsonov sindrom; Rothmund-Thomson-Syndrom; Hội chứng Rothmund–Thomson; Rothmund-Thomson syndrome; Ротмунд-Томсонов синдром; Rothmund–Thomsonin oireyhtymä; Rothmund-Thomsonov sindrom; condizione medica; Krankheit; maladie; مرض يصيب الإنسان; human disease; մարդու հիվանդություն; хвороба людини; наследственное заболевание; Синдром Ротмунда — Томсона; Congenital poikiloderma; RTS; Rothmund-Thomson syndrome (disorder); ROTHMUND-THOMSON SYNDROME; Poikiloderma Atrophicans and Cataract; ROTHMUND-THOMSON SYNDROME; RTS; Poikiloderma of Rothmund-Thomson; RTS; Ротмунд-Томпсонов синдром</nowiki>
Rothmund-Thomson syndrome human disease |
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| Instance of | - developmental defect during embryogenesis
- designated intractable/rare disease
- rare disease
- class of disease
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| Subclass of | - DNA repair-deficiency disorder
- skin disease
- photodermatosis
- hereditary neoplastic syndromes
- rare genetic developmental defect during embryogenesis
- hereditary poikiloderma
- ectodermal malformation syndrome associated with ocular features
- dentocutaneous disease with cataract
- progeroid syndrome
- genetic photodermatosis
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