ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

GM1 gangliosidosis type 1

Mucopolysaccharidosis type 4B

GLB1

Citations in the biomedical literature:

GM1 gangliosidosis type 1		Mucopolysaccharidosis type 4B
	Synonym(s): - Infantile GM1 gangliosidosis - Norman-Landing disease		Synonym(s): - Beta-D-galactosidase deficiency - MPSIVB - Morquio disease type B

	Classification (Orphanet): - Inborn errors of metabolism - Rare bone disease - Rare eye disease - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.