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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H01880 | Autosomal recessive microcephaly and chorioretinopathy | Autosomal-recessive microcephaly and chorioretinopathy (MCCRP) is a rare developmental disorder characterized by primary microcephaly, delayed psychomotor development, growth retardation with dwarfism ... | Congenital malformation |
(MCCRP1) TUBGCP6 [HSA:85378] [KO:K16573] (MCCRP2) PLK4 [HSA:10733] [KO:K08863] (MCCRP3) TUBGCP4 [HSA:27229] [KO:K16571] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |