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loading...| Preferred Name | Miller-Dieker lissencephaly syndrome | |
| Synonyms |
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| Definitions |
(MDLS): A contiguous gene deletion syndrome of chromosome 17p13.3, characterized by classical lissencephaly and distinct facial features. Additional congenital malformations can be part of the condition. |
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| ID |
http://purl.obolibrary.org/obo/OMIM_247200 |
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| definition |
(MDLS): A contiguous gene deletion syndrome of chromosome 17p13.3, characterized by classical lissencephaly and distinct facial features. Additional congenital malformations can be part of the condition. |
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| has_obo_namespace |
cell_cycle_ontology |
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| id |
OMIM:247200 |
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| label |
Miller-Dieker lissencephaly syndrome |
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| notation |
OMIM:247200 |
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| prefLabel |
Miller-Dieker lissencephaly syndrome |
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| treeView | ||
| subClassOf |
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