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Herb Integrative Database
Traditional Medicine Data Platform
Diseases

Type Ii Mucolipidosis

type ii mucolipidosis

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Entity Type
Diseases
Relation Groups
3
Relation Preview
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Basic Information

Grouped by core information, identifiers, and descriptions.

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Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Type Ii Mucolipidosis
Standard Disease Name
type ii mucolipidosis
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D009081
OMIM ID
252500|MTHU011301
UMLS ID
C0020725
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:An inherited lysosomal storage disease characterized by the presence of dense intracytoplasmic inclusions in mesenchymal cells, especially fibroblasts. Signs and symptoms include developmental delay, psychomotor deterioration, and growth failure.|CSP2006:rapidly progressing disease of young children, characterized histologically by abnormal fibroblasts containing a large number of dark inclusions which fill the central part of the cytoplasm except for the juxtanuclear zone (I cells), and clinically by severe growth impairment, minimal hepatomegaly, extreme mental and motor retardation, and clear corneas; inherited as an autosomal recessive trait, it is caused by failure of lysosomal enzymes to be incorporated into lysosomes.