GlyCosmos Portal

amyotrophic lateral sclerosis type 19

Synonym

Definition

An amyotrophic lateral sclerosis that has_material_basis_in mutation in the ERBB4 gene on chromosome 2.

Super Class

amyotrophic lateral sclerosis

Disease Ontology

DOID:0060210

Mondo Disease Ontology

OMIM

Related Genes

Displaying 1 entry
Gene ID	Gene Symbol	Description	Source
2066	ERBB4	erb-b2 receptor tyrosine kinase 4	Alliance of Genome Resources

Displaying 1 entry
Gene ID	Gene Symbol	Description	Source
13869	Erbb4	erb-b2 receptor tyrosine kinase 4	Alliance of Genome Resources

Displaying 1 entry
Gene ID	Gene Symbol	Description	Source
59323	Erbb4	erb-b2 receptor tyrosine kinase 4	Alliance of Genome Resources

Displaying 1 entry
Gene ID	Gene Symbol	Description	Source
37455	Egfr	Epidermal growth factor receptor	Alliance of Genome Resources

Displaying 1 entry
Gene ID	Gene Symbol	Description	Source
174462	let-23	Receptor tyrosine-protein kinase let-23;receptor protein-tyrosine kinase	Alliance of Genome Resources

Displaying entries **31 - 36** of 36 in total

« First

‹ Prev

1

2

3

4
HPO ID	HPO Term
HP:0004326	Cachexia
HP:0100543	Cognitive impairment
HP:0003484	Upper limb muscle weakness
HP:0009067	Progressive spinal muscular atrophy
HP:0003202	Skeletal muscle atrophy
HP:0007354	Amyotrophic lateral sclerosis

Displaying **all 6** entries
Gene ID	Gene Symbol	Description
5444	PON1	paraoxonase 1
5445	PON2	paraoxonase 2
5446	PON3	paraoxonase 3
55830	GLT8D1	glycosyltransferase 8 domain containing 1
7415	VCP	valosin containing protein
9896	FIG4	FIG4 phosphoinositide 5-phosphatase