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Xamoterol
Xanthelasma see Xanthelasma palpebrarum
Xanthelasma palpebrarum
Xanthelasmata see Xanthelasma palpebrarum
Xanthine alkaloids
Xanthine dehydrogenase deficiency see Xanthinuria type 1
Xanthine oxidase deficiency see Xanthinuria type 1
Xanthine oxidase inhibitor
Xanthinuria type 1
Xanthinuria type 2
Xanthochromia, CSF see CSF xanthochromia
Xanthogranulomatous pyelonephritis
Xanthoma see Xanthomata
Xanthoma of eyelid see Xanthelasma palpebrarum
Xanthoma tendinosum see Tendon xanthomata
Xanthomata
Xanthomata, eruptive see Eruptive cutaneous xanthomata
Xanthomatosis see Xanthomata
Xanthurenicaciduria see Hydroxykynureninuria
Xenoantibodies see Paul-Bunnell test positive
Xeroderma pigmentosum
Xeroderma pigmentosum group A
Xeroderma pigmentosum group B
Xeroderma pigmentosum group C
Xeroderma pigmentosum group D
Xeroderma pigmentosum group E
Xeroderma pigmentosum group F
Xeroderma pigmentosum group G
Xerophthalmia
Xerosis see Erythema craquele
Xerostomia
Ximelagatran
Xipamide
X-linked aqueductal stenosis see Hydrocephalus, X-linked
X-linked cone-rod dystrophy
X-linked dilated cardiomyopathy
X-linked hyperimmunoglobulin M syndrome
X-linked hypogammaglobulinaemia see Bruton agammaglobulinemia
X-linked hypophosphataemia
X-linked hypophosphatemic rickets see X-linked hypophosphataemia
X-linked ichthyosis
X-linked inheritance see X-linked inherited conditions
X-linked inherited conditions
X-linked liver glycogenosis see Glycogenosis type 8
X-linked lymphoproliferative disease
X-linked mental retardation 1 see Partington X-linked mental retardation syndrome
X-linked mental retardation 1 (non-specific) see Atkin-Flaitz-Patil syndrome
X-linked mental retardation syndrome type 5 see Pettigrew syndrome
X-linked mental retardation-hypotonic facies syndrome
X-linked myopathy with excessive autophagy
X-linked periventricular heterotopia
X-linked recessive nephrolithiasis type 1
X-linked recessive nephrolithiasis type 2 see Dent disease
X-linked severe combined immunodeficiency
X-linked sideroblastic anemia and ataxia
X-Linked spinal and bulbar atrophy see Kennedy disease
X-linked subcortical laminar heterotopia see Lissencephaly, X-linked
X-linked torsion dystonia-parkinsonism syndrome
X-linked visceral heterotaxy
XO syndrome see Turner syndrome
X-ray abnormality
XX male syndrome
XXY syndrome see Klinefelter syndrome
Xylitol
Xylitol dehydrogenase deficiency see Hereditary pentosuria
Xylometazoline
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