Item:Q21836: Difference between revisions

Created a new Item: orotic aciduria, pyrimidine metabolic disorder that is characterized by an excessive secretion of orotic acid in urine
 
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_30
 
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aliases / en / 0aliases / en / 0
 
Uridine monophosphate synthetase deficiency
aliases / en / 1aliases / en / 1
 
Oprt and Odc Deficiency
aliases / en / 2aliases / en / 2
 
Orotic Aciduria Without Megaloblastic Anemia
aliases / en / 3aliases / en / 3
 
Orotic Aciduria 1
aliases / en / 4aliases / en / 4
 
Orotidylic Pyrophosphorylase and Orotidylic Decarboxylase Deficiency
aliases / en / 5aliases / en / 5
 
Orotidylic decarboxylase deficiency
aliases / en / 6aliases / en / 6
 
Umps Deficiency
Property / instance of
 
Property / instance of: rare disease / rank
 
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Property / instance of: class of disease / rank
 
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Property / subclass of
 
Property / subclass of: pyrimidine metabolic disorder / rank
 
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Property / subclass of
 
Property / subclass of: vitamin B12- and folate-independent constitutional megaloblastic anemia / rank
 
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Property / health specialty
 
Property / health specialty: hematology / rank
 
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Property / exact match
 
Property / exact match: http://purl.obolibrary.org/obo/DOID_0050833 / rank
 
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Property / exact match
 
Property / exact match: http://identifiers.org/doid/DOID:0050833 / rank
 
Normal rank
Property / exact match
 
Property / exact match: http://www.orpha.net/ORDO/Orphanet_30 / rank
 
Normal rank