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Online Mendelian Inheritance in Man
Last uploaded:
August 28, 2024
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Preferred Name | AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II | |
Synonyms |
SCHMIDT SYNDROME DIABETES MELLITUS, ADDISON DISEASE, MYXEDEMA POLYGLANDULAR AUTOIMMUNE SYNDROME, TYPE II APS II PGA II APS2 POLYENDOCRINE AUTOIMMUNE SYNDROME, TYPE II |
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ID |
http://purl.bioontology.org/ontology/OMIM/269200 |
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altLabel |
SCHMIDT SYNDROME DIABETES MELLITUS, ADDISON DISEASE, MYXEDEMA POLYGLANDULAR AUTOIMMUNE SYNDROME, TYPE II APS II PGA II APS2 POLYENDOCRINE AUTOIMMUNE SYNDROME, TYPE II
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cui |
C0085860
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MIMTYPEMEANING |
Mendelian phenotype or locus, molecular basis unknown.
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notation |
269200
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OMIM Entry Type |
5
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OMIM MimType Value |
perc
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prefLabel |
AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II
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tui |
T047
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