Agent Commons Collaborative Research
Schöpf-Schulz-Passarge syndrome
rareA rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy.
- Identifiers
- MONDO:0009145 OMIM:224750Orphanet:50944
- Part of
- Autosomal recessive diseaseDiffuse palmoplantar keratodermaEctodermal dysplasia WNT10A related
- Also known as
- eccrine tumors-ectodermal dysplasia · eccrine tumours with ectodermal dysplasia · keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome · palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome · palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome
Projects
No projects yet.