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A genetic disorder characterized by the presence of multiple neurofibromas under the skin.
Definition source: English Wiktionary via Wiktextract
Usage: countable, uncountable
Topics: medicine, sciences
No example sentence was provided for this meaning.
Meaning relationships
Synonyms: none provided
Antonyms: none provided
autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities
Definition source: Princeton WordNet 3.0
No example sentence was provided for this meaning.
Meaning relationships
Synonyms: von Recklinghausen's disease
Antonyms: none provided
Broader terms: monogenic disorder, monogenic disease, autosomal dominant disease, autosomal dominant disorder
Etymology tree Proto-Indo-European *(s)neh1- Proto-Indo-European *-wr̥ Proto-Indo-European *snéh1wr̥der. Ancient Greek νεῦρον (neûron) Ancient Greek νευρο- (neuro-)der. English neuro- English fibroma English neurofibroma Proto-Indo-European *-tis Ancient Greek -τις (-tis) Ancient Greek -σῐς (-sĭs) Ancient Greek -ωσις (-ōsis)bor. New Latin -ōsislbor. English -osis English neurofibromatosis From neurofibroma + -osis.
Across languages
Translations
13 source translations are retained for this English entry.
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Catalan:
neurofibromatosi
— genetic disorder
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Danish:
neurofibromatose
— genetic disorder
-
Finnish:
neurofibromatoosi
— genetic disorder
-
French:
neurofibromatose
— genetic disorder
-
German:
Neurofibromatose
— genetic disorder
-
Hungarian:
neurofibromatózis
— genetic disorder
-
Italian:
neurofibromatosi
— genetic disorder
-
Polish:
nerwiakowłókniakowatość
— genetic disorder
-
Romanian:
neurofibromatoză
— genetic disorder
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Russian:
нѐйрофѝбромато́з
(nèjrofìbromatóz)
— genetic disorder
-
Spanish:
neurofibromatosis
— genetic disorder
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Thai:
แสนปม
(sɛ̌ɛn-bpom)
— genetic disorder
-
Ukrainian:
нейрофібромато́з
(nejrofibromatóz)
— genetic disorder