Craniofacial Abnormalities
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Stomach Neoplasms
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Breast Carcinoma
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Liver Cirrhosis, Experimental
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Endometriosis
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Lung Neoplasms
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Prostatic Neoplasms
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Mesothelioma, Malignant
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Tooth Abnormalities
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Carcinoma
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Urinary Bladder Neoplasms
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Gallbladder Neoplasm
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Cleft Lip
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Limb Deformities, Congenital
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Liver Cirrhosis
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Carcinoma, Adenoid Cystic
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Skin Neoplasms
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Coloboma
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Osteoarthritis
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Heart Defects, Congenital
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Heart Valve Diseases
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Hernia, Diaphragmatic
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Colonic Neoplasm
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Cyclopia
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Disease Progression
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Colorectal Cancer
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Mammary Neoplasms, Animal
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Mammary Neoplasms, Experimental
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Melanoma
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Peripheral Neuropathy
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Hepatocellular Carcinoma
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Craniosynostoses
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Squamous Cell Carcinoma
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Anodontia
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Acrocephalosyndactylia
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Respiratory System Abnormalities
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Myocardial Ischemia
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Eye Abnormalities
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Neoplasm Invasiveness
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Neoplasm Metastasis
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Endometrial Neoplasm
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Esophageal Neoplasms
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Exostoses, Multiple Hereditary
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Female Urogenital Diseases
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Fibrosis
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Glaucoma
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Griscelli Syndrome Type 1
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Hamartoma Syndrome, Multiple
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Hernias, Diaphragmatic, Congenital
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Holoprosencephaly 3
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Hypertension
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Hyperthyroidism
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Immunoblastic Lymphadenopathy
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Intellectual Disability
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Iridogoniodysgenesis, Dominant Type
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Jackson-Weiss Syndrome
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Jaw Abnormalities
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Kallmann Syndrome
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Kidney Neoplasms
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Lacrimoauriculodentodigital Syndrome
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Uterine Fibroid
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Lethal Congenital Contracture Syndrome 2
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Leukemia, Promyelocytic, Acute
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Liver Failure, Acute
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Furlong Syndrome
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Lymphatic Metastasis
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Lymphoma, Large B-Cell, Diffuse
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Lymphoma, Large-Cell, Anaplastic
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Lymphoma, Mantle-Cell
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Lymphoma, T-Cell
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Lymphoma, T-Cell, Cutaneous
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Lymphoma, T-Cell, Peripheral
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Microphthalmia, Isolated, With Coloboma 5
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Microphthalmia, Syndromic 2
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Microphthalmia, Syndromic 6
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Motor Skills Disorders
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Mouth Diseases
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Mouth Neoplasms
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Musculoskeletal Abnormalities
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Nasopharyngeal Carcinoma
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Nerve Degeneration
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Nervous System Diseases
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Obesity
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Odontoonychodermal Dysplasia
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Oligodontia-Colorectal Cancer Syndrome
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Oral Submucous Fibrosis
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Orofacial Cleft 11
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Orofacial Cleft 5
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Osteitis Deformans
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Osteogenesis Imperfecta, Type 2a
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Osteogenesis Imperfecta, Type 3
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Osteogenesis Imperfecta, Type 4
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Osteoporosis
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Osteosarcoma
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Ovarian Neoplasms
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Pain
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Parietal Foramina
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Parietal Foramina With Cleidocranial Dysplasia
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Parkinson Disease, Secondary
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Peters Anomaly
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Pfeiffer Type Acrocephalosyndactyly
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Plagiocephaly, Nonsynostotic
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Polycystic Kidney, Autosomal Recessive
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Preeclampsia
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Prolactinoma
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Proteinuria
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Recurrence
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Reperfusion Injury
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Ring Dermoid Of Cornea
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Saethre-Chotzen Syndrome With Eyelid Anomalies
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Salivary Gland Neoplasm
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Sarcoma, Clear Cell
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Scaphocephaly, Maxillary Retrusion, And Mental Retardation
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Schopf-Schulz-Passarge Syndrome
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Systemic Scleroderma
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Seizures
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Septic Shock
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Single Upper Central Incisor
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Skin Abnormalities
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Skin Diseases
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Spinal Cord Injuries
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Spinal Dysraphism
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Status Epilepticus
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Thyroid Diseases
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Tongue Neoplasms
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Tooth Agenesis, Selective, 3
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Tooth Agenesis, Selective, X-Linked, 1
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Ureteral Obstruction
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Urogenital Abnormalities
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Uterine Neoplasms
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Vitamin A Deficiency
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Witkop Syndrome
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22q11 Deletion Syndrome
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Wittwer Syndrome
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Abnormalities, Drug-Induced
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Abnormalities, Multiple
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Abortion, Spontaneous
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Acth-Secreting Pituitary Adenoma
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Adenocarcinoma
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Ankylosis
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Antley-Bixler Syndrome Phenotype
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Anxiety Disorder
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Thoracic Aortic Aneurysm
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Aortic Valve Insufficiency
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Arrhythmogenic Right Ventricular Dysplasia, Familial, 1
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Psoriatic Arthritis
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Rheumatoid Arthritis
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Asthma
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Autism
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Autoimmune Disease
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Bone Diseases, Developmental
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Burkitt Lymphoma
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Burns, Chemical
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Calcinosis
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Cardiovascular Abnormalities
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Cholangiocarcinoma
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Cholangitis
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Choledochal Cyst
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Ulcerative Colitis
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Craniofacial Dysostosis
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Craniosynostosis, Type 2
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Cutis Gyrata Syndrome Of Beare And Stevenson
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Cyanosis
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Deafness, Autosomal Dominant 39, With Dentinogenesis Imperfecta 1
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Dentinogenesis Imperfecta
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Dentinogenesis Imperfecta, Shields Type 3
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Diabetes Mellitus, Type 2
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Digeorge Syndrome
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Disease Models, Animal
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Ectodermal Dysplasia 1, Anhidrotic
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Edema, Cardiac
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Ehlers-Danlos Syndrome, Cardiac Valvular Form
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Ehlers-Danlos Syndrome, Type Vii, Autosomal Dominant
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