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Online Mendelian Inheritance in Man
Last uploaded:
January 16, 2025
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Id | http://purl.bioontology.org/ontology/OMIM/600122
http://purl.bioontology.org/ontology/OMIM/600122
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Preferred Name | VERLOES SYNDROME |
Synonyms |
MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE
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Type | http://www.w3.org/2002/07/owl#Class |
All Properties
altLabel | MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE
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prefLabel | VERLOES SYNDROME
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notation | 600122
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Scope Statement | X-linked inheritance possible [MISCELLANEOUS]
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OMIM MimType Value | none
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Has inheritance type | |
Semantic type UMLS property | |
OMIM Entry Type | 0
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type | |
Has manifestation |
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MIMTYPEMEANING | Other, mainly phenotypes with suspected mendelian basis
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tui | T047
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cui | C1838611
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