extremely rare and fatal autosomal recessive neurodegenerative disorder in humans
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rdf:type
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description
| - مرض يصيب الإنسان (ar)
- neurologinen sairaus (fi)
- extremely rare and fatal autosomal recessive neurodegenerative disorder in humans (en)
- disordine neurodegenerativo raro e fatale (it)
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exact match
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exact match
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health specialty
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ICD-10
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Mondo ID
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DiseasesDB
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ICPC 2 ID
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Disease Ontology ID
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Mondo ID
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health specialty
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ICD-10
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Mondo ID
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DiseasesDB
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ICPC 2 ID
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rdfs:label
| - Batenova bolest (sr)
- Batenova bolest (sh)
- Batenova bolest (sr-el)
- Battenin tauti (fi)
- Battenova bolest (bs)
- Choroba Spielmeyera-Vogta-Sjögrena (pl)
- Doença de Batten (pt)
- Enfermedad de Batten (es)
- Neuronale Ceroid-Lipofuszinose (de)
- Spielmeyer-Vogts sjukdom (sv)
- juvenile neuronal ceroid lipofuscinosis (en)
- maladie de Batten (fr)
- malattia di Batten (it)
- Батенова болест (mk)
- Батенова болест (sr-ec)
- Болезнь Баттена (ru)
- מחלת באטן (he)
- داء باتن (ar)
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skos:prefLabel
| - Batenova bolest (sr)
- Batenova bolest (sh)
- Batenova bolest (sr-el)
- Battenin tauti (fi)
- Battenova bolest (bs)
- Choroba Spielmeyera-Vogta-Sjögrena (pl)
- Doença de Batten (pt)
- Enfermedad de Batten (es)
- Neuronale Ceroid-Lipofuszinose (de)
- Spielmeyer-Vogts sjukdom (sv)
- juvenile neuronal ceroid lipofuscinosis (en)
- maladie de Batten (fr)
- malattia di Batten (it)
- Батенова болест (mk)
- Батенова болест (sr-ec)
- Болезнь Баттена (ru)
- מחלת באטן (he)
- داء باتن (ar)
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name
| - Batenova bolest (sr)
- Batenova bolest (sh)
- Batenova bolest (sr-el)
- Battenin tauti (fi)
- Battenova bolest (bs)
- Choroba Spielmeyera-Vogta-Sjögrena (pl)
- Doença de Batten (pt)
- Enfermedad de Batten (es)
- Neuronale Ceroid-Lipofuszinose (de)
- Spielmeyer-Vogts sjukdom (sv)
- juvenile neuronal ceroid lipofuscinosis (en)
- maladie de Batten (fr)
- malattia di Batten (it)
- Батенова болест (mk)
- Батенова болест (sr-ec)
- Болезнь Баттена (ru)
- מחלת באטן (he)
- داء باتن (ar)
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Freebase ID
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Freebase ID
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instance of
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instance of
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subclass of
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subclass of
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KEGG ID
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KEGG ID
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KEGG ID
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Orphanet ID
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genetic association
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ICD-10-CM
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PatientsLikeMe condition ID
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OMIM ID
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Orphanet ID
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genetic association
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