Leigh syndrome

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Leigh syndrome (256000) [OMIM:Leigh syndrome (256000)]
Leigh syndrome (in some patients) [OMIM:Leigh syndrome (in some patients)]
Quality:
Cross references:
OMIM: "Leigh syndrome" [OMIM:Leigh syndrome]
OMIM: "Leigh syndrome (256000)" [OMIM:Leigh syndrome (256000)]
OMIM: "Leigh syndrome (in some patients)" [OMIM:Leigh syndrome (in some patients)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

COENZYME Q10 DEFICIENCY, PRIMARY, 3 (OMIM:614652)
Combined oxidative phosphorylation defect type 14 (Orphanet:319519)
Combined oxidative phosphorylation defect type 15 (Orphanet:319524)
GRACILE syndrome (Orphanet:53693)
Isolated NADH-CoQ reductase deficiency (Orphanet:2609)
MEGDEL syndrome (Orphanet:352328)
Pyruvate dehydrogenase E3 deficiency (Orphanet:2394)