| dbo:description
|
- medical condition (en)
- медичний стан (uk)
|
| dbo:geneReviewsId
| |
| dbo:geneReviewsName
| |
| dbo:icd10
| |
| dbo:medicalDiagnosis
| |
| dbo:medicalSpecialty
| |
| dbo:orpha
| |
| dbo:thumbnail
| |
| dbo:wikiPageWikiLink
| |
| dbp:diagnosis
| |
| dbp:duration
| |
| dbp:frequency
|
- Unknown; HSAS 1 per 30,000 male live births (en)
|
| dbp:gard
| |
| dbp:genereviewsname
| |
| dbp:genereviewsnbk
| |
| dbp:icd
| |
| dbp:onset
| |
| dbp:orphanet
| |
| dbp:prognosis
|
- Varies depending on specific disorder (en)
|
| dbp:risks
| |
| dbp:specialty
| |
| dbp:synonyms
|
- L1CAM syndrome, CRASH syndrome, Corpus callosum hypoplasia-retardation-adducted thumbs-spasticity-hydrocephalus syndrome (en)
|
| dbp:treatment
| |
| dbp:wikiPageUsesTemplate
| |
| dct:subject
| |
| rdf:type
| |
| rdfs:label
|
- L1 syndrome (en)
- متلازمة L1 (ar)
|
| owl:sameAs
| |
| prov:wasDerivedFrom
| |
| foaf:depiction
| |
| foaf:isPrimaryTopicOf
| |
| is dbo:wikiPageRedirects
of | |
| is dbo:wikiPageWikiLink
of | |
| is foaf:primaryTopic
of | |
.jpg){kind=link}
.jpg){kind=link}
