OMOP Concept 4221555
Sex-linked hereditary disorder
StandardConditionSNOMED82852009Disorder
Maps from
3
Descendants
396
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
3 source codes normalize to Sex-linked hereditary disorder via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 113002 | Sex-linked hereditary disorder | Non-standard |
| CIEL | 113003 | Sex Linked Defects | Non-standard |
| MeSH | D025064 | Sex Chromosome Disorders | Non-standard |
Synonyms
Alternative names recorded for Sex-linked hereditary disorder across source vocabularies.
- Sex-linked hereditary disorder (disorder)
- trastorno hereditario ligado al sexo
- trastorno hereditario ligado al sexo (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(396)Included automatically when you query with descendants.
- 1Macular retinoschisis
- 1Opitz-Frias syndrome
- 1Ornithine carbamoyltransferase deficiency
- 1X-linked hereditary disease
- 2Absent radius, anogenital anomalies syndrome
- 2Adrenoleukodystrophy
- 2Adrenomyodystrophy
- 2Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome
- 2Ataxia with deafness and intellectual disability syndrome
- 2Atypical Rett syndrome
- 2Beta-propeller protein-associated neurodegeneration
- 2Dilated cardiomyopathy 3B
- 2Fabry's disease
- 2Familial x-linked hypophosphatemic vitamin D refractory rickets
- 2GATA binding protein 1 related thrombocytopenia with dyserythropoiesis
- 2Glucose-6-phosphate dehydrogenase deficiency anemia
- 2Hereditary factor IX deficiency disease
- 2Hereditary factor VIII deficiency disease
- 2Hypohidrotic X-linked ectodermal dysplasia
- 2Lissencephaly type 1 due to doublecortin gene mutation
- 2Macular and peripheral retinoschisis
- 2Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome
- 2MECP2 related disorder
- 2Oculo-palato-digital syndrome
- 2Ogden syndrome
Showing 25 of 396. Retrieve the full set via the API.
Get this concept via the API
Resolve Sex-linked hereditary disorder - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/4221555?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card