Incoming and outgoing links Dyskeratosis congenita
Back to articleIncoming links
- Atrophia cutis reticularis cum pigmentatione, dystrophia unguium et leukoplakia oris
- Berlin syndrome
- Cole buzzkill-toomey syndrome
- Cole-engmann syndrome
- Cole, harold newton
- DKC1 Gene
- Dyskeratosis, congenital
- Eye diseases, skin changes
- Familial cancer syndrome
- Fanconi-zinsser syndrome
- Hoyeraal-Hreidarsson syndrome
- Hypotrichosis
- Interest rate cole-engman syndrome
- Interest rate, ferdinand
- Kindler syndrome
- Mage-a3
- Neutropenia
- Onychodysplasia congenital of the index finger
- Onychodystrophy (overview)
- PID
- Poikilodermia vascularis atrophicans
- Polydysplasia ectodermica type cole buzzkill-toomey
- Primary immunodeficiencies and skin
- Reticular hyperpigmentations
- Teleangiectasia
- Teleangiectasia
- Telomerase
- TERT Gene
- Tumor syndromes, hereditary
Outgoing links
- 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
- Hyperhidrosis (overview)
- Hyperkeratosis
- Leukokeratosis
- Mage-a3
- Molgramostim
- Pachyonychia congenita
- Perlèche (overview)
- Pigment incontinence
- Poikiloderma (overview)
- Poikilodermia vascularis atrophicans
- Rothmund-thomson syndrome
- Telomerase
- TERT Gene