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Online Mendelian Inheritance in Man
Last uploaded:
August 28, 2024
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Preferred Name | LEIOMYOMA, UTERINE | |
Synonyms |
UL |
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ID |
http://purl.bioontology.org/ontology/OMIM/150699 |
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altLabel |
UL
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cui |
C0042133
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Has manifestation | ||
MIMTYPEMEANING |
Phenotype description, molecular basis known.
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notation |
150699
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|
OMIM Entry Type |
3
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|
OMIM MimType Value |
pound
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prefLabel |
LEIOMYOMA, UTERINE
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Scope Statement |
Caused by fusion of RAD51B (602948) and HMGIC (600698) genes [MOLECULAR BASIS] Uterine leiomyomata are found in hereditary leiomyomatosis and renal cell cancer syndrome (150800) [MISCELLANEOUS]
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tui |
T191
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