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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00991 | Microcephalic osteodysplastic primordial dwarfism, type II (MOPD II) | Microcephalic osteodysplastic primordial dwarfism, type II (MOPD II) is an autosomal recessive condition characterized by severe intrauterine and postnatal growth failure, microcephaly, and disproportionate ... | Congenital malformation | PCNT [HSA:5116] [KO:K16481] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |