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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02381 | Cleft palate, psychomotor retardation, and distinctive facial features | ... features, skeletal anomalies, and cognitive impairment. It has been reported that de novo mutations in KDM1A cause this disease. KDM1A is a histone demethylase that has been shown to play diverse and key ... | Congenital malformation | KDM1A [HSA:23028] [KO:K11450] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |