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Mucopolysaccharidosis type 2, severe form

1 associated gene
No signs/symptoms info

COMMON GENES: 1

Mucopolysaccharidosis type 2, attenuated form

1 associated gene
No signs/symptoms info

Mucopolysaccharidosis type 2, severe form

Mucopolysaccharidosis type 2, attenuated form

IDS

(UniProt - OMIM)

IDS

(UniProt - OMIM)


COMMON GENES	IDS

Citations in the biomedical literature:

Mucopolysaccharidosis type 2, severe form		Mucopolysaccharidosis type 2, attenuated form
	Synonym(s): - Hunter syndrome type A - Iduronate 2-sulfatase deficiency type A - Mucopolysaccharidosis type 2A		Synonym(s): - Hunter syndrome type B - Iduronate 2-sulfatase deficiency type B - Mucopolysaccharidosis type 2B

	Classification (Orphanet): - Inborn errors of metabolism - Rare bone disease - Rare cardiac disease - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare skin disease		Classification (Orphanet): - Inborn errors of metabolism - Rare bone disease - Rare cardiac disease - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare skin disease

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

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: young adult Type of inheritance: x-linked recessive		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: adult Type of inheritance: x-linked recessive

	External references: No OMIM references No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.