infantile-onset ascending hereditary spastic paralysis
Infantile-onset ascending hereditary spastic paralysis (IAHSP) is a very rare motor neuron disease characterized by severe spasticity of the lower limbs in early life, progression of spasticity to the upper limbs in late childhood, and dysarthria
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infantile-onset ascending hereditary spastic paralysis
Summary
infantile-onset ascending hereditary spastic paralysis is a rare disease[1].
Key Facts
- infantile-onset ascending hereditary spastic paralysis's instance of is recorded as rare disease[2].
- infantile-onset ascending hereditary spastic paralysis's instance of is recorded as class of disease[3].
- infantile-onset ascending hereditary spastic paralysis's subclass of is recorded as motor neuron disease[4].
- infantile-onset ascending hereditary spastic paralysis's subclass of is recorded as genetic motor neuron disease[5].
- infantile-onset ascending hereditary spastic paralysis's MeSH descriptor ID is recorded as C537217[6].
- infantile-onset ascending hereditary spastic paralysis's OMIM ID is recorded as 607225[7].
- infantile-onset ascending hereditary spastic paralysis's ICD-10 ID is recorded as G12.2[8].
- infantile-onset ascending hereditary spastic paralysis's KEGG ID is recorded as H01172[9].
- infantile-onset ascending hereditary spastic paralysis's Orphanet ID is recorded as 293168[10].
- infantile-onset ascending hereditary spastic paralysis's ICD-9-CM is recorded as 343.8[11].
- infantile-onset ascending hereditary spastic paralysis's health specialty is recorded as neurology[12].
- infantile-onset ascending hereditary spastic paralysis's genetic association is recorded as ALS2[13].
- infantile-onset ascending hereditary spastic paralysis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_293168[14].
- infantile-onset ascending hereditary spastic paralysis's UMLS CUI is recorded as C1846588[15].
- infantile-onset ascending hereditary spastic paralysis's UMLS CUI is recorded as C2931441[16].
- infantile-onset ascending hereditary spastic paralysis's ICD-10-CM is recorded as G12.2[17].
- infantile-onset ascending hereditary spastic paralysis's GARD rare disease ID is recorded as 4914[18].
- infantile-onset ascending hereditary spastic paralysis's Mondo ID is recorded as MONDO_0011797[19].
- infantile-onset ascending hereditary spastic paralysis's Genetics Home Reference Conditions ID is recorded as infantile-onset-ascending-hereditary-spastic-paralysis[20].
- infantile-onset ascending hereditary spastic paralysis's UniProt disease ID is recorded as DI-01823[21].