Catalog
Syndromes with skin or mucosal anomalies as a major feature
Link to WHO Definition
Syndromes with skin or mucosal anomalies as a major feature – http://id.who.int/icd/entity/1819307779
Parents
Children
- Ascher syndrome
- H syndrome
- LD27.0 Ectodermal dysplasia syndromes
- LD27.6 Genetic lipodystrophy
- LD27.1 Xeroderma pigmentosum
- LD27.4 Genetic syndromes affecting nails
- Pachyonychia congenita
- EC40 Pseudoxanthoma elasticum
- Cutis verticis gyrata - retinitis pigmentosa - sensorineural deafness
- Aplasia cutis congenita - intestinal lymphangiectasia
- 5C64.20 Acrodermatitis enteropathica
- Xeroderma pigmentosum-Cockayne syndrome complex
- LD27.5 Genetic hamartoneoplastic syndromes affecting the skin
- Lipoid proteinosis
- Aplasia cutis - myopia
- LD27.3 Genetic syndromes with hypertrichosis
- Palmoplantar keratoderma – oral leukokeratosis – oesophageal carcinoma
- LD27.2 Syndromic ichthyosis
- Xeroderma pigmentosum variant
- Cutis verticis gyrata - intellectual deficit
- Neuroectodermal melanolysosomal disease
- Hereditary acrokeratotic poikiloderma, Weary type
- Hereditary ichthyosis