Leukocyte Adhesion Deficiency, Type Iii,Combined Immunodeficiency,Autoimmune Lymphoproliferative Syndrome,Fibrosclerosis Of Breast,Lupus Erythematosus,Leukocyte Adhesion Deficiency, Type I,Bleeding Disorder, Platelet-Type, 18,Immunodeficiency 64,Systemic Lupus Erythematosus,Lymphoproliferative Syndrome

Neural Tube Closure Defect,Colorectal Cancer,Hepatocellular Carcinoma,Neural Tube Defects,Hyperoxaluria, Primary, Type Ii

Refractory Celiac Disease,Dermatitis Herpetiformis,Ulcerative Colitis,Celiac Disease 4,Inflammatory Bowel Disease,Inflammatory Bowel Disease 5,Inflammatory Bowel Disease 6,Colitis,Jejunoileitis,Celiac Disease 1

Heart Septal Defect,Heart Disease,Lung Cancer Susceptibility 3,Pulmonary Valve Stenosis,Atrial Heart Septal Defect,Neurofibromatosis-Noonan Syndrome,Neuroma,Hypertrophic Cardiomyopathy,Rasopathy,Noonan Syndrome-Like Disorder With Loose Anagen Hair,Keratosis Pilaris Atrophicans Faciei,Costello Syndrome,Joubert Syndrome 3,Neurofibromatosis, Type I,Villonodular Synovitis,Pilocytic Astrocytoma,Fibromatosis,Cryptorchidism, Unilateral Or Bilateral,Skin Granular Cell Tumor,Pseudo-Turner Syndrome,Noonan Syndrome 1,Noonan Syndrome And Noonan-Related Syndrome,Dilated Cardiomyopathy,Aortic Valve Disease 1,Gingival Hypertrophy,Noonan Syndrome-Like Disorder With Loose Anagen Hair 2,Adenocarcinoma,Neurofibromatosis,Breast Cancer,Patent Foramen Ovale,Colorectal Cancer,Gingival Overgrowth,Pulmonary Valve Disease,Hepatocellular Carcinoma,Cardiofaciocutaneous Syndrome 1,Embryonal Rhabdomyosarcoma,Rhabdomyosarcoma,Noonan Syndrome With Multiple Lentigines,Noonan Syndrome 3,Gingival Disease,Prostate Cancer,Keratosis Pilaris Atrophicans,Noonan Syndrome 4,Prostate Transitional Cell Carcinoma,Fibromatosis, Gingival, 1,Tetralogy Of Fallot,Epilepsy, Familial Temporal Lobe, 8,Patent Ductus Arteriosus 1,Ptosis,Juvenile Myelomonocytic Leukemia,Gingival Fibromatosis,Lung Cancer,Pulmonic Stenosis

Heart Septal Defect,Heart Disease,Lung Cancer Susceptibility 3,Pulmonary Valve Stenosis,Atrial Heart Septal Defect,Neurofibromatosis-Noonan Syndrome,Neuroma,Hypertrophic Cardiomyopathy,Rasopathy,Noonan Syndrome-Like Disorder With Loose Anagen Hair,Keratosis Pilaris Atrophicans Faciei,Costello Syndrome,Joubert Syndrome 3,Neurofibromatosis, Type I,Villonodular Synovitis,Pilocytic Astrocytoma,Fibromatosis,Cryptorchidism, Unilateral Or Bilateral,Skin Granular Cell Tumor,Pseudo-Turner Syndrome,Noonan Syndrome 1,Noonan Syndrome And Noonan-Related Syndrome,Dilated Cardiomyopathy,Aortic Valve Disease 1,Gingival Hypertrophy,Noonan Syndrome-Like Disorder With Loose Anagen Hair 2,Adenocarcinoma,Neurofibromatosis,Breast Cancer,Patent Foramen Ovale,Colorectal Cancer,Gingival Overgrowth,Pulmonary Valve Disease,Hepatocellular Carcinoma,Cardiofaciocutaneous Syndrome 1,Embryonal Rhabdomyosarcoma,Rhabdomyosarcoma,Noonan Syndrome With Multiple Lentigines,Noonan Syndrome 3,Gingival Disease,Prostate Cancer,Keratosis Pilaris Atrophicans,Noonan Syndrome 4,Prostate Transitional Cell Carcinoma,Fibromatosis, Gingival, 1,Tetralogy Of Fallot,Epilepsy, Familial Temporal Lobe, 8,Patent Ductus Arteriosus 1,Ptosis,Juvenile Myelomonocytic Leukemia,Gingival Fibromatosis,Lung Cancer,Pulmonic Stenosis

Benign Epilepsy With Centrotemporal Spikes,Prader-Willi Syndrome,Chromosome 15q13.3 Deletion Syndrome

Developmental And Epileptic Encephalopathy 4

Exotropia,Anisometropia,Hypertropia,Accommodative Esotropia,Esotropia,Hypotropia,Duane Retraction Syndrome,Binocular Vision Disease,Abnormal Retinal Correspondence,Autosomal Dominant Robinow Syndrome,Ocular Motility Disease,Dandy-Walker Syndrome,Sensorineural Hearing Loss,Night Blindness,Suppression Amblyopia,Amblyopia,Ametropic Amblyopia,Diaphragmatic Eventration,Diaphragm Disease,Paralytic Squint,Partial Third-Nerve Palsy,Abducens Nerve Disease,Tukel Syndrome,Hydronephrosis,Cleft Palate, Isolated,Duane Retraction Syndrome 2,Duane Retraction Syndrome 1,Strabismus,Nonaka Myopathy,Robinow Syndrome, Autosomal Dominant 2,Marden-Walker Syndrome,Duane-Radial Ray Syndrome,Laryngomalacia,Robinow Syndrome,Congenital Ptosis

Lung Cancer

Neuroblastoma,Borna Disease,Chromosome 17q23.1-Q23.2 Deletion Syndrome,Disease Of Mental Health,Bartter Syndrome, Type 2, Antenatal,Johanson-Blizzard Syndrome,Jacobsen Syndrome

Mast-Cell Leukemia,Mastocytosis,Bleeding Disorder, Platelet-Type, 18,Asthma

Noma,Microphthalmia,Dent Disease 1,Non-Syndromic X-Linked Intellectual Disability,Lowe Oculocerebrorenal Syndrome

Leukocyte Adhesion Deficiency, Type Iii,Hemorrhagic Disease,Combined Immunodeficiency,Glanzmann Thrombasthenia,Leukocyte Adhesion Deficiency, Type I,Thrombocytopenia,Bleeding Disorder, Platelet-Type, 18,Stormorken Syndrome

Diverticulitis,Diverticulitis Of Colon,Meier-Gorlin Syndrome 2,Bladder Squamous Cell Carcinoma,Mowat-Wilson Syndrome,Epilepsy, Idiopathic Generalized 9