Incoming and outgoing links Poikiloderma (overview)
Back to articleIncoming links
- Amyloidosis cutaneous special forms
- Baller-Gerold syndrome
- Berlin syndrome
- Dyskeratosis congenita
- Dysplasia, congenital ectodermal with cataract
- Familial cancer syndrome
- Hartnup syndrome
- Interface dermatitis
- Lower leg pigmentation, hereditary atrophy associated with atrophy
- Poikiloderma, acquired
- Poikiloderma, actinic
- Poikiloderma, congenital
- Poikiloderma, congenital
- Poikiloderma, congenital with warty hyperkeratosis
- Poikiloderma, thermal
- Poikilodermatomyositis
- Postinflammatory hyperpigmentation
- Progeria adultorum
- Prolidase deficiency
- Rapadilino syndrome
- Reticular hyperpigmentations
- Rothmund syndrome
- Rothmund-thomson syndrome
- Thomson syndrome
- Xeroderma pigmentosum
Outgoing links
- Acrodermatitis chronica atrophicans
- Baller-Gerold syndrome
- BLM Gene
- Bloom syndrome
- Dermatomyositis (overview)
- Dyskeratosis congenita
- Dysplasia, congenital ectodermal with cataract
- Erythema
- Goltz syndrome
- Graft-versus-host disease chronic
- Hartnup syndrome
- Incontinentia pigmenti (Bloch-Sulzberger)
- Kindler syndrome
- Lichen planus classic type
- Lupus erythematosus systemic
- Maculopapular cutaneous mastocytosis
- Mycosis fungoides
- Poikiloderma, actinic
- Poikiloderma, congenital with warty hyperkeratosis
- Poikiloderma, thermal
- Poikiloderma with neutropenia
- Progeria adultorum
- Radiodermatitis chronic
- Retiform parakeratosis
- Riehl melanosis
- Rothmund syndrome
- Rothmund-thomson syndrome
- Scleroderma systemic
- Thomson syndrome