Sex-linked hereditary disorder
|
X-linked hereditary disease (disorder)
X-linked hereditary disease
X-gebonden hereditaire aandoening
X-gebonden erfelijke ziekte
Id128430005
StatusPrimitive
ICD-10 complex map reference set
Target
RuleTRUE
AdviceMAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
CorrelationSNOMED CT source code to target map code correlation not specified
|
Absent radius, anogenital anomalies syndrome
Adrenomyodystrophy
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome
Ataxia with deafness and intellectual disability syndrome
Atypical Rett syndrome
Beta-propeller protein-associated neurodegeneration
Dilated cardiomyopathy 3B
Fabry's disease
Familial x-linked hypophosphatemic vitamin D refractory rickets1
Female restricted epilepsy with intellectual disability syndrome
GATA binding protein 1 related thrombocytopenia with dyserythropoiesis
Glucose-6-phosphate dehydrogenase deficiency anemia6
Hereditary factor IX deficiency disease5
Hereditary factor VIII deficiency disease5
Hereditary nephrogenic diabetes insipidus
Hereditary nephrogenic diabetes insipidus
Hypohidrotic X-linked ectodermal dysplasia
Lissencephaly type 1 due to doublecortin gene mutation
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome
Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
Oculo-palato-digital syndrome
Ogden syndrome
Ohdo syndrome, Maat-Kievit-Brunner type
Pelizaeus-Merzbacher disease8
Placental sulfatase deficiency
Placental sulfatase deficiency
Seemanova Lesny syndrome
Solute carrier family 35 member A2 congenital disorder of glycosylation
Wilson Turner syndrome
X-linked absence of thyroxine-binding globulin
X-linked agammaglobulinemia
X-linked asexual dwarfism
X-linked chronic granulomatous disease
X-linked cleft palate and ankyloglossia
X-linked creatine deficiency
X-linked creatine deficiency
X-linked distal hereditary motor neuropathy3
X-linked dominant erythropoietic protoporphyria
X-linked dominant hereditary disease34
X-linked dyskeratosis congenita1
X-linked excess of thyroxine-binding globulin
X-linked hereditary motor and sensory neuropathy6
X-linked hereditary spastic paraplegia4
X-linked hypodontia
X-linked hypoparathyroidism
X-linked intellectual disability Brooks type
X-linked intellectual disability Turner type
X-linked intellectual disability Wilson type
X-linked intellectual disability, craniofacioskeletal syndrome
X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome
X-linked lethal multiple pterygium syndrome
X-linked muscular dystrophy not predominantly limb girdle
X-linked muscular dystrophy with limb girdle distribution2
X-linked oligodontia
X-linked optic atrophy1
X-linked panhypopituitarism
X-linked periventricular heterotopia
X-linked recessive hereditary disease194
X-linked reduction of thyroxine-binding globulin
X-linked retinitis pigmentosa3
X-linked sensorineural hearing loss6
X-linked variant form of thyroxine-binding globulin
Xq25 microduplication syndrome