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Experimental Factor Ontology
Last uploaded:
November 18, 2024
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Preferred Name | lattice corneal dystrophy | |
Synonyms |
lattice corneal dystrophy familial amyloid neuropathy, Finnish type lattice corneal dystrophy (disease) |
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ID |
http://purl.obolibrary.org/obo/MONDO_0004686 |
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database_cross_reference |
MEDGEN:56355 SCTID:1192004 UMLS:C0155127 icd11.foundation:1247885635 ICD9:277.39 DOID:8943 HP:0001149 ICD9:357.4
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exactMatch |
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1247885635 http://identifiers.org/snomedct/1192004 http://linkedlifedata.com/resource/umls/id/C0155127 |
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has_exact_synonym |
lattice corneal dystrophy familial amyloid neuropathy, Finnish type lattice corneal dystrophy (disease)
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IAO_0000589 |
lattice corneal dystrophy (disease)
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|
id |
MONDO:0004686
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in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-base#rare |
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label |
lattice corneal dystrophy
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|
notation |
MONDO:0004686
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preferred label |
lattice corneal dystrophy
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|
prefLabel |
lattice corneal dystrophy
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subClassOf | ||
excluded_subClassOf |
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