X-linked complicated corpus callosum dysgenesis
medical condition
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Summary
X-linked complicated corpus callosum dysgenesis is a rare disease[1]. It draws 27 Wikipedia views per month (rare disease category, ranking #237 of 627).[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: disease[4]
- Said to be the same as: L1 syndrome[5]
- Prevalence: 0.000001[6]
- Genetic association: L1CAM[7]
- Age of onset: congenital onset[8], neonatal onset[9]
- Exact match: http://www.orpha.net/ORDO/Orphanet_1497[10], http://www.orpha.net/ORDO/Orphanet_275543[11]
- Has phenotype: global developmental delay[12], flat feet[13], Ventriculomegaly[14], disability affecting intellectual abilities[15], seizure[16], microcephaly[17], spasticity[18], cerebellar hypoplasia[19], muscle weakness[20], High-arched palate[21], strabismus[22], Q141815059[23], Hirschsprung's disease[24], Q141815249[25]
- P14914: D01497[26]