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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/141300
http://purl.bioontology.org/ontology/OMIM/141300
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Preferred Name | HEMIFACIAL ATROPHY, PROGRESSIVE |
Synonyms |
HFA
PARRY-ROMBERG SYNDROME
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Type | http://www.w3.org/2002/07/owl#Class |
All Properties
altLabel |
HFA
PARRY-ROMBERG SYNDROME
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prefLabel | HEMIFACIAL ATROPHY, PROGRESSIVE
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notation | 141300
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Scope Statement |
Left sided involvement occurs more frequently [MISCELLANEOUS]
Onset in childhood or early adulthood [MISCELLANEOUS]
Majority of cases are sporadic [MISCELLANEOUS]
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OMIM MimType Value | perc
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Has inheritance type | |
Semantic type UMLS property | |
OMIM Entry Type | 5
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type | |
Has manifestation |
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MIMTYPEMEANING | Mendelian phenotype or locus, molecular basis unknown.
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tui | T047
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cui | C0015458
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