PCD Karyotype Amylose AA Management NLRC4 NLRP3 Biopsy Inflammation A20 haploinsufficiency COVID-19 Infant Genetic counselling Amyloidosis Bronchiectasis Diagnosis Pulmonary fibrosis Mutations CRISPR-Cas9 Biopsie Mutation Autoinflammatory syndrome Prognosis Primary ciliary dyskinesia CCDC39 Pituitary Cilia Genetics Infertility Serum amyloid A Genetic analysis Familial mediterranean fever ICSI Rare diseases Turner syndrome Surfactant Idiopathic pulmonary fibrosis Mosaic Cystic fibrosis ABCA3 Adrenal tumors Adipokines Mortality Phenotype Dynein arm assembly Rare lung diseases Intellectual disability Paediatric interstitial lung disease Human TNFAIP3 AA amyloidosis Male infertility Colchicine Osteosarcoma Common interstitial lung disease Vasculitis Familial Mediterranean fever France Pneumopathie interstitielle diffuse AL amyloidosis Inflammasome Atherosclerosis Male Pregnancy Cytokines Autoimmunity Biomarkers Insulin resistance Electron microscopy TRAPS Adolescent TCF4 GHRHR TNFRSF1A Lipodystrophy NGS MEFV Humans Founder effect Sarcoidosis Classification Maladies auto-inflammatoires Interstitial lung disease Pyrine Situs inversus Female Fièvre méditerranéenne familiale Autoinflammation Pyrin Pulmonary hypertension Autoinflammatory disease Fibrose pulmonaire Kartagener syndrome Children Lung function Premature ovarian insufficiency Interleukine 1 Dynein SARS-CoV-2 Cohort