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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00500 | Keutel syndrome | Keutel syndrome is a rare autosomal recessive condition characterized by diffuse cartilage calcification. Mutations in the matrix Gla protein gene (MGP) have been reported. | Congenital malformation | MGP [HSA:4256] [KO:K19481] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |