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Results 1 - 10 of 38734 > >>
EC Number
Disease
PubMed ID
Title of Publication
Category
Confidence Level
4alpha-methylsterol monooxygenase deficiency
Disorders of sterol synthesis: beyond Smith-Lemli-Opitz syndrome.
causal interaction
3
4alpha-methylsterol monooxygenase deficiency
Disorders of sterol synthesis: beyond Smith-Lemli-Opitz syndrome.
therapeutic application
1
4alpha-methylsterol monooxygenase deficiency
Disorders of sterol synthesis: beyond Smith-Lemli-Opitz syndrome.
unassigned
0
Abetalipoproteinemia
Histochemical and ultrastructural pathology of skeletal muscle in a patient with abetalipoproteinemia.
causal interaction
3
Abetalipoproteinemia
Clinicopathological study of familial late infantile Hallervorden-Spatz disease: a particular form of neuroacanthocytosis.
causal interaction
1
Abetalipoproteinemia
A novel frameshift mutation in the McLeod syndrome gene in a Japanese family.
causal interaction
3
Abetalipoproteinemia
A case of McLeod syndrome with unusually severe myopathy.
causal interaction
3
Abetalipoproteinemia
Kell, Kx and the McLeod syndrome.
causal interaction
2
Abetalipoproteinemia
Abnormal accumulation of tTGase products in muscle and erythrocytes of chorea-acanthocytosis patients.
causal interaction
1
Abetalipoproteinemia
McLeod syndrome: a neurohaematological disorder.
causal interaction
4
Results 1 - 10 of 38734 > >>