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loading...| Preferred Name |
Morquio Syndrome |
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| Synonyms |
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| Definitions |
A rare autosomal recessive lysosomal storage disease characterized by abnormal skeletal developments, dwarfism, heart disorders, and central nervous system deficits. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C61263 |
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| code |
C61263 |
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| Contributing_Source |
Cellosaurus |
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| definition |
A rare autosomal recessive lysosomal storage disease characterized by abnormal skeletal developments, dwarfism, heart disorders, and central nervous system deficits. |
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| in_subset | ||
| label |
Morquio Syndrome |
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| Legacy Concept Name |
Morquio_Syndrome |
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| Preferred_Name |
Morquio Syndrome |
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| prefixIRI |
NCIT:C61263 |
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| prefLabel |
Morquio Syndrome |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0026707 |
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| subClassOf |
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