Incoming and outgoing links Xeroderma pigmentosum
Back to articleIncoming links
- Atrophodermia pigmentosa
- Back mutation
- Basal cell carcinomatosis
- Cockayne syndrome
- De sanctis-cacchione syndrome
- Dna repair
- Dna repair genes
- Dyschromatosis universalis hereditaria
- Ephelids
- ERCC2 Gene
- Eye diseases, skin changes
- Familial cancer syndrome
- Fibroxanthoma atypical
- Kaposi, moriz
- Lentigines syndromes
- Lioderma essentialis congenita
- Neurom fibrillar
- Photocarcinogenesis
- Pibi(d)s syndrome
- Plant tars
- Porphyria erythropoetica congenita
- REV1 gene
- Senilitas cutis praecox
- Spot darker
- Teleangiectasia
- Teleangiectasia
- Trichothiodystrophy
- Tumor syndromes, hereditary
- Xerodermoid, pigmented
Outgoing links
- Acitretin
- Actinic keratosis
- Atrophy of the skin (overview)
- Basal cell carcinoma (overview)
- Cryosurgery
- Curettage
- Darian sign
- Dermis
- De sanctis-cacchione syndrome
- Dna repair
- Dyschromia
- Ectropium
- Excision
- Familial atypical multiple birthmark and melanoma syndrome (FAMM)
- Goltz syndrome
- Hydroa vacciniforme
- Isotretinoin
- Kaposi, moriz
- Light protection
- Light stabilizers
- Lupus erythematosus systemic
- Maculopapular cutaneous mastocytosis
- Melanoma cutaneous
- Microstomy
- Peutz-jeghers syndrome
- Phenotype
- Poikiloderma (overview)
- Polymorphic light eruption
- Porphyria erythropoetica congenita
- Progeria adultorum
- Retinoids
- REV1 gene
- Scale
- Squamous cell carcinoma of the skin
- Stratum basale
- Translesion DNA synthesis
- Xerodermoid, pigmented