L1 syndrome
hereditary spastic paraplegia that is characterized by hydrocephalus, spasticity of the lower limbs, adducted thumbs, aphasia, seizures, agenesis of the corpus callosum and intellectual disability in the mild to moderate range
Press Enter · cited answer in seconds
0 sources
L1 syndrome
Summary
L1 syndrome is a class of disease[1]. It draws 77 Wikipedia views per month (class_of_disease category, ranking #619 of 1,968).[2]
Key Facts
- L1 syndrome's instance of is recorded as class of disease[3].
- L1 syndrome is a type of X-linked intellectual disability[4].
- L1 syndrome is a type of hereditary spastic paraplegia[5].
- L1 syndrome is a type of X-linked complex spastic paraplegia[6].
- L1 syndrome is a type of nervous system heredodegenerative disease[7].
- L1 syndrome is a type of X-linked recessive disease[8].
- L1 syndrome's said to be the same as is recorded as L1 syndrome[9].
- L1 syndrome's NCI Thesaurus ID is recorded as C129930[10].
- L1 syndrome's health specialty is recorded as neurology[11].
- L1 syndrome's genetic association is recorded as L1CAM[12].
- L1 syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060246[13].
- L1 syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060246[14].
- L1 syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2466[15].
- L1 syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_275543[16].
- L1 syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
L1 syndrome draws 77 Wikipedia views per month (class_of_disease category, ranking #619 of 1,968).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[18] It is known by 15 alternative names across languages and contexts.[19]