amyotrophic lateral sclerosis type 4
human disease
Press Enter · cited answer in seconds
0 sources
Summary
amyotrophic lateral sclerosis type 4 is a rare disease[1]. It is known by 11 alternative names across languages and contexts.[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: amyotrophic lateral sclerosis[4], nervous system heredodegenerative disease[5], genetic motor neuron disease[6]
- Prevalence: 0.000001[7]
- Health specialty: neurology[8]
- Genetic association: SETX[9]
- Age of onset: juvenile onset[10], childhood onset[11]
- Exact match: http://purl.obolibrary.org/obo/DOID_0060196[12], http://identifiers.org/doid/DOID:0060196[13], http://www.orpha.net/ORDO/Orphanet_357043[14]
- On focus list of Wikimedia project: WikiProject Medicine[15]
- Has phenotype: Q141815174[16], skeletal muscle atrophy[17], Babinski sign[18], pyramidal sign[19], paraplegia[20], gait abnormality[21], pes cavus[22], clonus[23], hypoesthesia[24]
- P14914: D357043[25]