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oculomotor, with congenital contractures and muscle atrophy apraxia
|
C536703 |
|
|
pancreatic hypoplasia diabetes heart disease
|
C536714 |
|
|
hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome
|
C536742 |
|
|
wiedemann grosse dibbern syndrome
|
C536704 |
|
|
x-linked immunoneurologic disorder
|
C536743 |
|
|
macrocephaly and dysplastic nails pectus excavatum
|
C536728 |
|
|
brachial amelia, forebrain defects, and facial clefts
|
C536713 |
|
|
multiple, with early-onset diabetes mellitus epiphyseal dysplasia
|
C536739 |
|
|
chromosome xq duplication syndrome
|
C536732 |
|
|
x chromosome, duplication xq13 1 q21 1
|
C536753 |
|
|
hirsutism, skeletal dysplasia, mental retardation syndrome
|
C536705 |
|
|
iranian variant form mucolipidosis III
|
C565367 |
|
|
severe intrauterine growth retardation with increased mitomycin c sensitivity
|
C536744 |
|
|
hyperostosis corticalis generalisata congenita
|
C536748 |
|
|
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus
|
C536748 |
|
