Property:Has condition inheritance

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Showing 12 pages using this property.
C
Charcot Marie Tooth Disease +
Autosomal dominant  +
E
Erythromelalgia +
Primary disease: Autosomal dominant  +
F
Fabry Disease +
X-linked  +
Facioscapulohumeral Dystrophy +
Autosomal dominant (FSHD 1), digenic (FSHD 2)  +
Familial Episodic Pain Syndrome +
Heterozygous  +
L
Loeys-Dietz Syndrome +
Autosomal dominant  +
M
McArdle Disease +
Autosomal recessive  +
Myotonia Congenita +
Autosomal dominant (Thomsen) or recessive (Becker)  +
Myotonic Dystrophy +
Autosomal dominant  +
P
Paroxysmal Extreme Pain Disorder +
Autosomal dominant  +
Pompe Disease +
Autosomal recessive  +
T
Tarui Disease +
Autosomal recessive  +
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