|
neurodegeneration with brain iron accumulation due to C19orf12 mutation
|
13674 |
|
|
neurodegeneration with brain iron accumulation type 4
|
13674 |
|
|
subendocardial myocardial infarction
|
3674 |
|
|
osteosclerosis, autosomal dominant worth type with torus palatinus
|
C536748 |
|
|
severe intrauterine growth retardation with increased mitomycin c sensitivity
|
C536744 |
|
|
benign hyperostosis corticalis generalisata
|
C536748 |
|
|
hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome
|
C536742 |
|
|
x-linked immunoneurologic disorder
|
C536743 |
|
|
hyperostosis corticalis generalisata congenita
|
C536748 |
|
|
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus
|
C536748 |
|
|
woolly hair, hypotrichosis, everted lower lip and outstanding ears
|
C536746 |
|
|
woolly hair, hypotrichosis, everted lower lip, and outstanding ears
|
C536746 |
|
|
benign form of worth, with torus palatinus hyperostosis corticalis generalisata
|
C536748 |
|
