ZFIN Human Disease: amyotrophic lateral sclerosis type 1

OBO ID: DOID:0060193

Term Name:	amyotrophic lateral sclerosis type 1		Search Ontology:
Synonyms:	ALS1 amyotrophic lateral sclerosis 1
Definition:	An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SOD1 gene on chromosome 21. The most common type of familial ALS. http://en.wikipedia.org/wiki/Amyotrophic_lateral_sclerosis
References:	ICD10CM:G12.2 OMIM:105400
Ontology:	Human Disease ( DOID:0060193 )

Relationships

is a type of:	amyotrophic lateral sclerosis autosomal dominant disease autosomal recessive disease amyotrophic lateral sclerosis autosomal dominant disease autosomal recessive disease Show first 5 Terms

OTHER amyotrophic lateral sclerosis type 1 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
DCTN1	dctn1b dctn1a	{Amyotrophic lateral sclerosis, susceptibility to}	105400
PRPH	prph	{Amyotrophic lateral sclerosis, susceptibility to}	105400
SOD1	sod1	Amyotrophic lateral sclerosis 1	105400
NEFH		{?Amyotrophic lateral sclerosis, susceptibility to}

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None