X-linked hereditary disease
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X-linked dominant hereditary disease (disorder)
X-linked dominant hereditary disease
X-gebonden hereditaire dominante aandoening
X-gebonden erfelijke dominante ziekte
Id1162984000
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
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2-methyl-3-hydroxybutyric aciduria
Adrenoleukodystrophy3
Aicardi's syndrome
Alport syndrome X-linked1
Atkin Flaitz syndrome
BRESEK syndrome
CASK related intellectual disability
Chondrodysplasia punctata, X-linked dominant type
CLCN4-related X-linked intellectual disability syndrome
Craniofrontonasal dysplasia
Familial infantile gigantism1
Focal dermal hypoplasia
Fragile X associated tremor ataxia syndrome
Fragile X syndrome
Incontinentia pigmenti syndrome
Lisch epithelial corneal dystrophy
Microphthalmia with linear skin defect syndrome
Nance-Horan syndrome
Oculofaciocardiodental syndrome
Otopalatodigital syndrome spectrum disorder5
PPM-X syndrome
Skeletal dysplasia brachydactyly syndrome
STAR syndrome
Torticollis, keloids, cryptorchidism, renal dysplasia syndrome
X-linked Charcot-Marie-Tooth disease type 1
X-linked Charcot-Marie-Tooth disease type 6
X-linked congenital generalized hypertrichosis
X-linked dominant chondrodysplasia Chassaing Lacombe type
X-linked dominant erythropoietic protoporphyria
X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability
X-linked immunoneurologic disorder
X-linked intellectual disability with cerebellar hypoplasia syndrome
X-linked reticulate pigmentary disorder with systemic manifestation syndrome
X-linked scapuloperoneal muscular dystrophy