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MCID: MCP034
MIFTS: 12
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Mucopolysaccharidosis Type 2, Attenuated Form
Categories:
Neuronal diseases, Eye diseases, Bone diseases, Skin diseases, Metabolic diseases, Fetal diseases, Rare diseases
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MalaCards integrated aliases for Mucopolysaccharidosis Type 2, Attenuated Form:
Name: Mucopolysaccharidosis Type 2, Attenuated Form
59
Characteristics:Orphanet epidemiological data:59
mucopolysaccharidosis type 2, attenuated form
Inheritance: X-linked recessive; Age of onset: Childhood; Age of death: adult; Classifications:
MalaCards categories:
Global: Metabolic diseases Fetal diseases Rare diseases Anatomical: Neuronal diseases Eye diseases Bone diseases Skin diseases
ICD10:
34
Orphanet: 59
Rare neurological diseases
Rare eye diseases
Rare bone diseases
Rare skin diseases
Inborn errors of metabolism
Developmental anomalies during embryogenesis
External Ids:
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MalaCards based summary
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Mucopolysaccharidosis Type 2, Attenuated Form, also known as mucopolysaccharidosis type ii, attenuated form, is related to mucopolysaccharidosis, type ii. An important gene associated with Mucopolysaccharidosis Type 2, Attenuated Form is IDS (Iduronate 2-Sulfatase). Affiliated tissues include skin, bone and eye.
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Diseases related to Mucopolysaccharidosis Type 2, Attenuated Form via text searches within MalaCards or GeneCards Suite gene sharing:
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MalaCards organs/tissues related to Mucopolysaccharidosis Type 2, Attenuated Form:41
Skin,
Bone,
Eye
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Search
GEO
for disease gene expression data for Mucopolysaccharidosis Type 2, Attenuated Form.
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