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PMO Precision Medicine Ontology
Last uploaded:
December 16, 2020
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Id | http://www.phoc.org.cn/pmo/class/PMO_00039953
http://www.phoc.org.cn/pmo/class/PMO_00039953
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Preferred Name | 22q11 Deletion Syndrome |
Definitions |
A chromosomal disease that has_material_basis_in deletion polymorphisms at chromosome location 22q11 and is characterized by variable developmental problems and schizoid features.
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Type | http://www.w3.org/2002/07/owl#Class |
All Properties
label |
22q11 Deletion Syndrome
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prefLabel |
22q11 Deletion Syndrome
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Synonym |
Syndromes, 22q11 Deletion
22q11 Deletion Syndrome [Disease/Finding]
Deletion Syndrome, 22q11
22q11 Deletion Syndromes
Deletion Syndromes, 22q11
Syndrome, 22q11 Deletion
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Definition |
A chromosomal disease that has_material_basis_in deletion polymorphisms at chromosome location 22q11 and is characterized by variable developmental problems and schizoid features.
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PMOID |
PMO:00039953
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MCID |
MC00797860
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prefixIRI |
pmo:PMO_00039953
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Database_Cross_Reference |
NDFRT:N0000182241
MSH:D058165
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Tree Number |
T9.5.1.5.1
T9.8.3.10.1
T9.8.3.1.29
T9.20.1.3.4
T9.8.3.3.1.4
T9.3.6.8.6
T9.8.4.32.9
T9.8.3.7.8.6
T9.20.3.1.4
T9.9.10.2.1
T9.8.3.9.9
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subClassOf |
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type |
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