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