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bn:00912533n
Noun Concept
IT
No term available
EN
Antley–Bixler syndrome is a rare, severe autosomal recessive congenital disorder characterized by malformations and deformities affecting the majority of the skeleton and other areas of the body. Wikipedia
Relations
Sources
IS A
malattia rara
malattia autosomica recessiva
GENETIC ASSOCIATION
POR
FGFR2
HAS CAUSE
EN
cytochrome P450 Oxidoreductase Deficiency
HEALTH SPECIALTY
genetica clinica
SYMPTOMS
craniostenosi

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