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Entry | Name | Description | Category | Pathway | Gene |
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H00838 | Congenital fibrosis of the extraocular muscles | Congenital fibrosis of the extraocular muscles (CFEOM) describes a group of rare congenital eye movement disorders that result from the dysfunction of all or part of the oculomotor (CN 3) and the trochlear ... | Nervous system disease |
(CFEOM1, CFEOM3B) KIF21A [HSA:55605] [KO:K24185] (CFEOM2) PHOX2A [HSA:401] [KO:K09330] (CFEOM3A) TUBB3 [HSA:10381] [KO:K07375] (CFEOM5) COL25A1 [HSA:84570] [KO:K24356] |
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H01881 | Complex cortical dysplasia with other brain malformations | Complex cortical dysplasia with other brain malformations (CDCBM) is a disorder of aberrant neuronal migration and disturbed axonal guidance. Patients exhibit mental retardation, strabismus combined with ... | Congenital malformation |
(CDCBM1) TUBB3 [HSA:10381] [KO:K07375] (CDCBM2) KIF5C [HSA:3800] [KO:K10396] (CDCBM3) KIF2A [HSA:3796] [KO:K10393] (CDCBM4) TUBG1 [HSA:7283] [KO:K10389] (CDCBM5) TUBB2A [HSA:7280] [KO:K07375] (CDCBM6) TUBB [HSA:203068] [KO:K07375] (CDCBM7) TUBB2B [HSA:347733] [KO:K07375] (CDCBM9) CTNNA2 [HSA:1496] [KO:K05691] (CDCBM10) APC2 [HSA:10297] [KO:K02085] (CDCBM11) KIF26A [HSA:26153] [KO:K10404] (CDCBM12) CAMSAP1 [HSA:157922] [KO:K17493] (CDCBM13) DYNC1H1 [HSA:1778] [KO:K10413] |
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