OMOP Concept 37160643
X-linked dominant hereditary disease
StandardConditionSNOMED1162984000Disorder
Maps from
0
Descendants
45
Valid from
30 Sept 2021
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for X-linked dominant hereditary disease across source vocabularies.
- enfermedad hereditaria dominante ligada al cromosoma X
- enfermedad hereditaria dominante ligada al cromosoma X (trastorno)
- X-linked dominant hereditary disease (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(6)Roll up to these when you need a wider cohort.
Narrower concepts
(45)Included automatically when you query with descendants.
- 12-methyl-3-hydroxybutyric aciduria
- 1Aicardi's syndrome
- 1Alport syndrome X-linked
- 1Atkin Flaitz syndrome
- 1BRESEK syndrome
- 1CASK related intellectual disability
- 1CHILD syndrome
- 1Chondrodysplasia punctata, X-linked dominant type
- 1CLCN4-related X-linked intellectual disability syndrome
- 1Craniofrontonasal dysplasia
- 1Danon disease
- 1Familial infantile gigantism
- 1Focal dermal hypoplasia
- 1Fragile X associated tremor ataxia syndrome
- 1Fragile X syndrome
- 1Incontinentia pigmenti syndrome
- 1Lisch epithelial corneal dystrophy
- 1Microphthalmia with linear skin defect syndrome
- 1Nance-Horan syndrome
- 1Oculofaciocardiodental syndrome
- 1Otopalatodigital syndrome spectrum disorder
- 1PPM-X syndrome
- 1Rett syndrome
- 1Skeletal dysplasia brachydactyly syndrome
- 1STAR syndrome
- 1Torticollis, keloids, cryptorchidism, renal dysplasia syndrome
- 1X-linked Charcot-Marie-Tooth disease type 1
- 1X-linked Charcot-Marie-Tooth disease type 6
- 1X-linked congenital generalized hypertrichosis
- 1X-linked dominant chondrodysplasia Chassaing Lacombe type
- 1X-linked dominant erythropoietic protoporphyria
- 1X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability
- 1X-linked immunoneurologic disorder
- 1X-linked intellectual disability, hypotonia, movement disorder syndrome
- 1X-linked intellectual disability with cerebellar hypoplasia syndrome
- 1X-linked reticulate pigmentary disorder with systemic manifestation syndrome
- 1X-linked scapuloperoneal muscular dystrophy
- 2Frontometaphyseal dysplasia
- 2Melnick-Needles syndrome
- 2Oto-palato-digital syndrome, type I
- 2Oto-palato-digital syndrome, type II
- 2Symptomatic form of fragile X syndrome in female carrier
- 2Terminal osseous dysplasia and pigmentary defect syndrome
- 2X-linked acrogigantism due to Xq26 microduplication
- 2X-linked diffuse leiomyomatosis with Alport syndrome
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