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X chromosome, duplication Xq13 1 q21 1 |
X chromosome, monosomy Xp22 pter |
X chromosome, monosomy Xq28 |
X chromosome, trisomy Xp3 |
X chromosome, trisomy Xpter Xq13 |
X chromosome, trisomy Xq |
X chromosome, trisomy Xq25 |
X fragile site folic acid type |
X linked Juvenile Retinoschisis |
X linked Lymphoproliferative Syndrome |
Xanthic urolithiasis |
Xanthine oxydase deficiency |
Xanthinuria |
Xanthomatosis cerebrotendinous |
Xanthophobia |
Xenoglossophobia |
Xenophobia |
Xerocytosis, hereditary |
Xeroderma Pigmentosum |
Xeroderma pigmentosum, type 1 |
Xeroderma pigmentosum, type 2 |
Xeroderma pigmentosum, type 3 |
Xeroderma pigmentosum, type 5 |
Xeroderma pigmentosum, type 6 |
Xeroderma pigmentosum, type 7 |
Xeroderma pigmentosum, variant type |
Xeroderma talipes enamel defects |
Xerophobia |
Xk aprosencephaly |
X-linked adrenal hypoplasia congenita |
X-linked alpha thalassemia mental retardation syndrome (ATR-X) |
X-linked dominant |
X-linked ichthyosis |
X-linked juvenile retinoschisis |
X-linked juvenile retinoschisis |
X-linked lymphoproliferative syndrome |
X-linked mental retardation and macro-orchidism |
X-linked mental retardation associated with marXq2 |
X-linked mental retardation Brooks type |
X-linked mental retardation craniofacial abnormal microcephaly club |
X-linked mental retardation De silva type |
X-linked mental retardation Hamel type |
X-linked mental retardation type Gustavson |
X-linked mental retardation type Martinez |
X-linked mental retardation type Raynaud |
X-linked mental retardation type Schutz |
X-linked mental retardation type Snyder |
X-linked mental retardation type Wittner |
X-linked mental retardation-hypotonia |
X-linked severe combined immunodeficiency |
X-linked trait |
XX male syndrome |
XY Female |
XY gonadal agenesis syndrome |
Xylophobia |
XYY Syndrome |