dermatopathia pigmentosa reticularis
human disease
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dermatopathia pigmentosa reticularis
Summary
dermatopathia pigmentosa reticularis is a developmental defect during embryogenesis[1].
Key Facts
- dermatopathia pigmentosa reticularis's instance of is recorded as developmental defect during embryogenesis[2].
- dermatopathia pigmentosa reticularis's instance of is recorded as rare disease[3].
- dermatopathia pigmentosa reticularis's instance of is recorded as class of disease[4].
- dermatopathia pigmentosa reticularis is a type of pigmentation disorder[5].
- dermatopathia pigmentosa reticularis is a type of hyperpigmentation of the skin[6].
- dermatopathia pigmentosa reticularis is a type of autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature[7].
- dermatopathia pigmentosa reticularis is a type of autosomal dominant disease[8].
- dermatopathia pigmentosa reticularis is a type of ectodermal dysplasia[9].
- dermatopathia pigmentosa reticularis's health specialty is recorded as medical genetics[10].
- dermatopathia pigmentosa reticularis's genetic association is recorded as KRT14[11].
- dermatopathia pigmentosa reticularis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_86920[12].
- dermatopathia pigmentosa reticularis's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111342[13].
- dermatopathia pigmentosa reticularis's exact match is recorded as http://identifiers.org/doid/DOID:0111342[14].