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bn:00057409n
Noun Concept
SYL
No term available
EN
Autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities WordNet 3.0
Relations
Sources
IS A
EN
autosomal dominant disease
EN
monogenic disorder
EN
disease
EN
rare disease
EN
neurofibromatosis
+2 relations
HAS KIND
EN
neurofibromatosis
EN
Neurofibromatosis type 3
EN
Neurofibromatosis type 4
EN
neurofibromatosis type II
EN
schwannomatosis
+1 relations
GENETIC ASSOCIATION
EN
neurofibromin 2
EN
neurofibromin 1
HEALTH SPECIALTY
EN
neurology
EN
medical genetics
MODE OF INHERITANCE
EN
autosomal dominant
POSSIBLE MEDICAL FINDINGS
EN
Crowe sign

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