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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/613456
http://purl.bioontology.org/ontology/OMIM/613456
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Preferred Name | FRONTONASAL DYSPLASIA 3 |
Synonyms |
FND3
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Type | http://www.w3.org/2002/07/owl#Class |
All Properties
altLabel | FND3
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prefLabel | FRONTONASAL DYSPLASIA 3
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Gene Symbol |
FND3
ALX1
CART1
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notation | 613456
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Scope Statement | Caused by mutation in aristaless-like homeobox 1 (ALX1, 601527.0001) [MOLECULAR BASIS]
Variable expressivity [MISCELLANEOUS]
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OMIM MimType Value | pound
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Has inheritance type | |
Semantic type UMLS property | |
OMIM Entry Type | 3
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type | |
Has manifestation |
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MIMTYPEMEANING | Phenotype description, molecular basis known.
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Gene Locus | 12q21.3-q22
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tui | T047
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cui | C3150706
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