|
carnitine uptake deficiency
|
C536778 |
|
|
systemic carnitine deficiency
|
C536778 |
|
|
EMERY-Dreifuss muscular dystrophy 7, autosomal dominant
|
13677 |
|
|
yemenite (warburg) deaf-blind hypopigmentation syndrome
|
C536771 |
|
|
TMEM43 autosomal dominant Emery-Dreifuss muscular dystrophy
|
13677 |
|
|
Emery-Dreifuss muscular dystrophy 7, autosomal dominant
|
13677 |
|
|
EMERY-Dreifuss muscular dystrophy 7, autosomal dominant; EDMD7
|
http://purl.obolibrary.org/obo/MONDO_0013677 |
|
|
yemenite deaf-blind hypopigmentation syndrome
|
C536771 |
|
|
lateral myocardial infarction
|
3677 |
|
|
carnitine deficiency, primary
|
C536778 |
|
|
plasma-membrane, deficiency of carnitine transporter
|
C536778 |
|
|
carnitine transporter, plasma-membrane, deficiency of
|
C536778 |
|
|
carnitine deficiency, systemic primary
|
C536778 |
|
