ORPHA:56965

Progressive bulbar paralysis of childhood

Synonyms: Fazio-Londe disease · Progressive bulbar palsy of childhood

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Riboflavin transporter deficiency

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Progressive bulbar paralysis of childhood	Fazio-Londe disease · Progressive bulbar palsy of childhood
fr	Paralysie bulbaire progressive de l'enfant	Maladie de Fazio-Londe
de	Progressive Bulbärparalyse des Kindesalters	Fazio-Londe-Krankheit
es	Parálisis bulbar progresiva de la infancia	Enfermedad de Fazio-Londe
it	Paralisi bulbare progressiva dell'infanzia	Malattia di Fazio-Londe
nl	Progressieve bulbaire paralyse in de kinderjaren	Ziekte van Fazio-Londe
pt	Paralisia bulbar progressiva da infância	Doença de Fazio-Londe
pl	Postępujący opuszkowy paraliż dziecięcy	Choroba Fazio i Londe
cs	Progresivní bulbární paralýza v dětství	Fasiova-Londeho nemoc · Progresivní bulbární ochrnutí v dětství
uk	Прогресуючий бульбарний параліч дитячого віку	Хвороба Фаціо-Лонде · Прогресуючий дитячий бульбарний параліч
zh	儿童进行性延髓麻痹	儿童期进行性延髓麻痹
tr	Çocukluk çağında ilerleyici bulber paralizi	Fazio-Londe hastalığı · Çocukluk çağı ilerleyici bulbar felci

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MeSH	D010244	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Not placed in any Orphanet classification in this release.

No children.

0 direct

Orphanet records no gene directly on this code.

0 records

No prevalence record in this release.

Orphanet has no HPO annotation for this code in this release.