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Diseases
Aplasia Cutis Congenita, Nonsyndromic
aplasia cutis congenita, nonsyndromic
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- Aplasia Cutis Congenita, Nonsyndromic
- Standard Disease Name
- aplasia cutis congenita, nonsyndromic
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- No data
- OMIM ID
- 107600
- UMLS ID
- C0282160|C2931779
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:Localized or widespread congenital absence of skin. The lesions most frequently occur in the scalp, are well demarcated, may be superficial or deep, and are not associated with inflammation.|HPO2016_07_04:A developmental defect resulting in the congenital absence of skin in multiple or solitary non-inflammatory, well-demarcated, oval or circular ulcers with a diameter of about 1 to 2 cm. Aplasia cutis congenita most commonly occurs on the scalp, but may present in the face, trunk, or limbs. [HPO:probinson]