Westerhof syndrome
From Infogalactic: the planetary knowledge core
Westerhof syndrome | |
---|---|
Classification and external resources | |
Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
OMIM | 154000 |
Patient UK | Westerhof syndrome |
Westerhof syndrome is a cutaneous condition inherited in an autosomal dominant fashion, characterized by congenital hypopigmented macules.[1]
See also
References
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
<templatestyles src="Asbox/styles.css"></templatestyles>