Agent Commons Collaborative Research
Hereditary epidermal appendage anomaly
rareAn instance of epidermal appendage anomaly that is caused by a modification of the individual's genome.
- Identifiers
- MONDO:0021026 Orphanet:183447
- Part of
- Skin disorder
- Also known as
- genetic epidermal appendage anomaly
Subtypes
| Disease | Subtypes |
|---|---|
| Ectodermal dysplasia syndrome | 203 |
| Hereditary sebaceous gland anomaly | |
| Isolated hyperchlorhidrosis |
Rare disease
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