Disease list starting with X
Diseases Database
Disease, medication, symptom etc database index : X
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's 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 lymphoproliferative disease
X-linked mental retardation 1
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's disease
X-linked severe combined immunodeficiency
X-linked sideroblastic anemia and ataxia
X-Linked spinal and bulbar atrophy see Kennedy's disease
X-linked torsion dystonia-parkinsonism syndrome
X-linked visceral heterotaxy
XO syndrome see Turner's syndrome
X-ray abnormality
XX male syndrome
XXY syndrome see Klinefelter syndrome
Xylitol
Xylitol dehydrogenase deficiency see Hereditary pentosuria
Xylometazoline
Disease, medication, symptom etc database index : X
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's 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 lymphoproliferative disease
X-linked mental retardation 1
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's disease
X-linked severe combined immunodeficiency
X-linked sideroblastic anemia and ataxia
X-Linked spinal and bulbar atrophy see Kennedy's disease
X-linked torsion dystonia-parkinsonism syndrome
X-linked visceral heterotaxy
XO syndrome see Turner's syndrome
X-ray abnormality
XX male syndrome
XXY syndrome see Klinefelter syndrome
Xylitol
Xylitol dehydrogenase deficiency see Hereditary pentosuria
Xylometazoline
1 Comments:
At January 26, 2010 at 10:40 PM , Medical Information said...
Xeroderma Pigmentosum is very rare skin disorder in which DNA damaged by UV light. It can cause skin cancer. Some of the symptoms are uneven dark patches on skin, skin drying, skin appearing thin etc. If anyone observes symptoms of it, should consult doctor immediately. For more information on it, refer Xeroderma Pigmentosum
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