ICD-10: Z14
Genetic carrier
Subcategories
Related Diseases
Danon disease
X-linked dominant hypophosphatemic rickets
autosomal dominant disease
non-syndromic X-linked intellectual disability
autosomal dominant hypophosphatemic rickets
autosomal recessive cerebellar ataxia
X-linked hereditary ataxia
spinocerebellar ataxia type 11
autosomal recessive spinocerebellar ataxia 10
familial juvenile hyperuricemic nephropathy
autosomal recessive pyridoxine-refractory sideroblastic anemia 2
syndromic X-linked intellectual disability
mitochondrial complex III deficiency nuclear type 2
hereditary papulotranslucent acrokeratoderma
X-linked cleft palate with or without ankyloglossia
autosomal dominant nocturnal frontal lobe epilepsy 1
autosomal dominant nocturnal frontal lobe epilepsy 2
autosomal dominant nocturnal frontal lobe epilepsy 5
Muenke Syndrome
syndromic X-linked intellectual disability Siderius type
Griscelli syndrome type 2
Griscelli syndrome type 3
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