| dbo:alias
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- Escalante syndrome (en)
- Martin–Bell syndrome, (en)
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| dbo:description
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- תסמונת גנטית (iw)
- maladie génétique (fr)
- congenital disorder of nervous system (en)
- vrozená vada nervové soustavy (cs)
- homa genetika malsano (eo)
- Erbkrankheit durch Mutation des X-Chromosoms (de)
- choroba genetyczna z mutacją chromosomu X (pl)
- malattia congenita del sistema nervoso (it)
- perinnöllinen sairaus (fi)
- trastorno genético (es)
- doença genética caracterizada por deficiência intelectual ligeira a moderada (pt)
- prirojena motnja živčnega sistema zaradi mutacije na kromosomu X (sl)
- ناهنجاری ژنتیکی سندرم ایکس شکننده (fa)
- 先天性神經系統疾病 (zh)
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- Boy with protruding ears, a characteristic of fragile X syndrome (en)
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| dbp:icd
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- 759.830000 (xsd:double)
- (en)
- Q99.2 (en)
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- Intellectual disability, long and narrow face, large ears, flexible fingers, autistic behavior, large testicles (en)
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| dbp:synonyms
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- Escalante syndrome (en)
- Martin–Bell syndrome, (en)
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| dbp:treatment
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- Supportive care, early interventions (en)
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| gold:hypernym
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| rdfs:label
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- Fragile X syndrome (en)
- Síndrome X fràgil (ca)
- Σύνδρομο ευθραύστου χρωματοσώματος X (el)
- متلازمة الكروموسوم إكس الهش (ar)
- Fragila X sindromo (eo)
- X hauskorraren sindrome (eu)
- Fragiles-X-Syndrom (de)
- Síndrome X frágil (es)
- Syndrome de l'X fragile (fr)
- Sindrome dell'X fragile (it)
- 脆弱X症候群 (ja)
- 취약 X 증후군 (ko)
- Fragiele-X-syndroom (nl)
- Zespół łamliwego chromosomu X (pl)
- Síndrome do X frágil (pt)
- Синдром Мартина — Белл (ru)
- Fragil X-syndromet (sv)
- X染色體易裂症 (zh)
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