molybdenum cofactor deficiency
(Q1621463)
metal metabolism disease characterized by encephalopathy that worsens over time resulting from the absence of molybdenum cofactor which leads to accumulation of toxic levels of sulphite and neurological damage
metal metabolism disease characterized by encephalopathy that worsens over time resulting from the absence of molybdenum cofactor which leads to accumulation of toxic levels of sulphite and neurological damage
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Current Data About
molybdenum cofactor deficiency
| (P31) |
(Q929833)
(Q112193867) |
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| (P279) |
(Q3281373)
|
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| (P1748) |
C129076
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| (P2293) |
(Q18029242)
|
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_0111165
http://identifiers.org/doid/DOID:0111165
http://www.orpha.net/ORDO/Orphanet_99732 |
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| (P5008) |
(Q4099686)
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other details
| aliases |
combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase MOCOD |
| description | metal metabolism disease characterized by encephalopathy that worsens over time resulting from the absence of molybdenum cofactor which leads to accumulation of toxic levels of sulphite and neurological damage |
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