Verweise von und zu Dyskeratosis congenita
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- Atrophia cutis reticularis cum pigmentatione, dystrophia unguium et leukoplakia oris
- Eye diseases, skin changes
- Berlin syndrome
- Cole-engmann syndrome
- Cole, harold newton
- Cole buzzkill-toomey syndrome
- DKC1 Gene
- Dyskeratosis, congenital
- Fanconi-zinsser syndrome
- Hoyeraal-Hreidarsson syndrome
- Hypotrichosis
- Primary immunodeficiencies and skin
- PID
- Kindler syndrome
- Mage-a3
- Neutropenia
- Onychodysplasia congenital of the index finger
- Onychodystrophy (overview)
- Poikilodermia vascularis atrophicans
- Polydysplasia ectodermica type cole buzzkill-toomey
- Reticular hyperpigmentations
- Teleangiectasia
- Teleangiectasia
- Telomerase
- TERT Gene
- Familial cancer syndrome
- Tumor syndromes, hereditary
- Interest rate cole-engman syndrome
- Interest rate, ferdinand
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- Anal fissure
- Anetoderma
- Anonychia (overview)
- Atrophy of the skin (overview)
- DKC1 Gene
- Ectropium
- Fanconi anaemia
- Fanconi-zinsser syndrome
- Graft-versus-host disease
- Granulocyte-macrophage colony stimulating factor
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- Hyperkeratosis
- Leukokeratosis
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- Pachyonychia congenita
- Perlèche (overview)
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- Poikiloderma (overview)
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