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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00883 |
Lipoid proteinosis Urbach-Wiethe disease |
Lipoid proteinosis (LP) is a rare autosomal recessive disorder characterized histologically by infiltration of periodic acid Schiff-positive hyaline material into the skin, upper aerodigestive tract, and ... | Congenital malformation | ECM1 [HSA:1893] [KO:K23867] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |