Leigh disease
(Q1815019)
mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity
mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity
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Current Data About
Leigh disease
| (P31) |
(Q929833)
(Q112193867) |
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| (P279) |
(Q935710)
(Q12136) |
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| (P373) |
Leigh syndrome
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| (P780) |
(Q127076)
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| (P1748) |
C84814
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| (P1995) |
(Q83042)
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| (P2293) |
(Q18029992)
(Q18029923)
(Q18042184)
(Q17847759)
(Q18029898)
(Q17909099)
(Q18029973)
(Q18056075)
(Q14907256)
(Q18029980)
(Q18031793)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_3652
http://identifiers.org/doid/DOID:3652
http://www.orpha.net/ORDO/Orphanet_506 |
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| (P5008) |
(Q4099686)
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other details
| aliases |
Infantile necrotizing encephalomyelopathy LEIGH SYNDROME Leigh's disease (disorder) juvenile subacute necrotizing encephalomyelopathy subacute necrotizing encephalomyelopathy |
| description | mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity |
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