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Diseases: X
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X chromosome, duplication Xq13 1 q21 1
X chromosome, monosomy Xp22 pter
X chromosome, monosomy Xq28
X chromosome, trisomy 26-28
X chromosome, trisomy Xp3
X chromosome, trisomy Xpter Xq13
X chromosome, trisomy Xq
X chromosome, trisomy Xq25
X-linked adrenal hypoplasia congenita
X-linked agammaglobulinemia
X-linked Hypophosphatemic Rickets
X-linked ichthyosis
X-Linked Lymphoproliferative Syndrome (XLP)
X-linked mental retardation and macro-orchidism
X-linked mental retardation associated with marXq2
X-linked mental retardation craniofacial abnormal microcephaly club
X-linked mental retardation De silva type
X-linked mental retardation Gustavson type
X-linked mental retardation type Martinez
X-linked mental retardation type Raynaud
X-linked mental retardation type Schutz
X-linked mental retardation type Wittwer
X-linked periventricular heterotopia
X-Linked Recessive Diseases
Xanthinuria type 1
Xanthinuria type 2
Xanthogranuloma
Xanthogranuloma, Juvenile
Xanthogranulomatous cholecystitis
Xanthogranulomatous sialadenitis
Xeroderma pigmentosum
Xeroderma pigmentosum type 7
Xeroderma pigmentosum, type 1
Xeroderma pigmentosum, type 2
Xeroderma pigmentosum, type 3
Xeroderma pigmentosum, type 5
Xeroderma pigmentosum, type 6
Xeroderma pigmentosum, type 9
Xeroderma pigmentosum, variant type
Xeroderma talipes enamel defects
XFE progeroid syndrome
XK aprosencephaly
XX male syndrome
XY Female
XY Pure Gonadal Dysgenesis
xyyz