X-linked bulbospinal neuropathy

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X-linked bulbospinal neuropathy,

a hereditary disorder of the spinal cord and medulla oblongata in males, with associated endocrine features, including azoospermia, gynecomastia, glucose intolerance, and feminized skin changes.

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X-chromosome
X-deletion X ovarian dysgenesis
X-inactivation
X-linkage
X-linked
X-linked adrenoleukodystrophy
X-linked agammaglobulinemia
X-linked bulbospinal neuropathy
X-linked centronuclear-myotubular myopathy
X-linked disorder
X-linked dominant inheritance
X-linked gene
X-linked hypogammaglobulinemia
X-linked hypophosphatemia
X-linked hypophosphatemic osteomalacia

X-League
X-Legged Sally
X-linkage
X-linked
X-linked
X-linked
X-linked
X-linked adrenal hypoplasia congenita
X-linked adrenoleukodystrophy
X-linked adrenoleukodystrophy
X-linked adrenoleukodystrophy
X-linked agammaglobinemia
X-linked agammaglobinemia
X-linked agammaglobulinaemia
X-linked agammaglobulinaemia
X-linked agammaglobulinemia

X-linked agammaglobulinemia
X-linked agammaglobulinemia
X-linked agammaglobulinemia
X-linked agammaglobulinemia
X-linked AHC
X-linked alpha thalassemia mental retardation syndrome
X-linked alpha thalassemia mental retardation syndrome (ATR-X)
X-Linked Autoimmunity-Allergic Disregulation
X-linked bulbospinal neuropathy
X-linked centronuclear-myotubular myopathy
X-Linked Chronic Granulomatous Disease
X-linked congenital stationary night blindness
X-linked congenital stationary night blindness
X-Linked Dilated Cardiomyopathy
X-linked disorder
X-linked dominant
X-linked dominant

X-linked dominant inheritance
X-linked dominant inheritance
X-linked dysplasia-gigantism syndrome
X-Linked Ectodysplasin Receptor
X-linked gene
X-linked gene
X-linked gene
X-linked gene
X-Linked Helicase 2
X-Linked Hyper IgM
X-Linked Hyper-IGM Immunodeficiency with Ectodermal Dysplasia
X-linked hypogammaglobulinemia
X-Linked Hypohidrotic Ectodermal Dysplasia
X-linked hypophosphataemia
X-linked hypophosphataemia
X-Linked Hypophosphataemic Rickets

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