Breast Carcinoma
|
Hypertension
|
Lung Neoplasms
|
Liver Cirrhosis, Experimental
|
Skin Neoplasms
|
Deafness, Autosomal Recessive 1a
|
Glioblastoma Multiforme
|
Adenoma
|
Deafness
|
Autism
|
Salivary Gland Neoplasm
|
Peripheral Neuropathy
|
Eye Abnormalities
|
Seizures
|
Status Epilepticus
|
Cataract
|
Hyperkeratosis, Epidermolytic
|
Fraser Syndrome
|
Erythrokeratodermia Variabilis
|
Carcinoma, Adenoid Cystic
|
Ectodermal Dysplasia
|
Hearing Loss, Sensorineural
|
Prostatic Neoplasms
|
Myocardial Reperfusion Injury
|
Carcinoma, Pancreatic Ductal
|
Cell Transformation, Neoplastic
|
Deafness, Autosomal Dominant 3a
|
Deafness, Autosomal Dominant 2b
|
Deafness, Autosomal Dominant 3b
|
Deafness, Autosomal Recessive 1b
|
Major Depression
|
Dermatitis, Allergic Contact
|
Dermatitis, Contact
|
Epidermolysis Bullosa
|
Epidermolysis Bullosa, Junctional
|
Epidermolysis Bullosa, Junctional, Non-Herlitz Type
|
Epidermolysis Bullosa Simplex
|
Epidermolysis Bullosa With Pyloric Atresia
|
Facies
|
Febrile Convulsions, Familial, 4
|
Fibrosarcoma
|
Glioma
|
Gliosis
|
Hallermann's Syndrome
|
Heart Defects, Congenital
|
Heart Failure
|
Hemangiosarcoma
|
Hereditary Renal Agenesis
|
Hernia, Diaphragmatic
|
Hernias, Diaphragmatic, Congenital
|
Hidradenitis Suppurativa
|
Hid Syndrome
|
Hirschsprung Disease
|
Allergy
|
Hypoplastic Left Heart Syndrome
|
Ichthyosis
|
Intellectual Disability
|
Keratitis
|
Keratitis, Ichthyosis, And Deafness (Kid) Syndrome
|
Keratoderma, Palmoplantar
|
Knuckle Pads, Leuconychia And Sensorineural Deafness
|
Learning Disorders
|
Leigh Disease
|
Leukemia, Myeloid, Acute
|
Leukemia, Myelomonocytic, Juvenile
|
Leukodystrophy, Hypomyelinating, 2
|
Liposarcoma
|
Liver Neoplasms
|
Liver Neoplasms, Experimental
|
Lymphangioleiomyomatosis
|
Macrostomia
|
Maple Syrup Urine Disease
|
Marles Greenberg Persaud Syndrome
|
Megacolon
|
Melanoma
|
Meningioma
|
Movement Disorder
|
Myocardial Ischemia
|
Myopia
|
Neoplasm Invasiveness
|
Neoplasm Metastasis
|
Nerve Sheath Neoplasms
|
Neurilemmoma
|
Neurofibroma
|
Neurofibromatoses
|
Neurofibromatosis 1
|
Neurofibromatosis, Familial Spinal
|
Neurofibromatosis-Noonan Syndrome
|
Nevus, Pigmented
|
Oculodentodigital Dysplasia
|
Oculodentodigital Dysplasia, Autosomal Recessive
|
Ovarian Cysts
|
Pain
|
Palmoplantar Keratoderma With Deafness
|
Pheochromocytoma
|
Pneumonia
|
Polycystic Ovary Syndrome
|
Precancerous Conditions
|
Proteinuria
|
Psoriasis
|
Pyloric Atresia
|
Recurrence
|
Refractive Errors
|
Reperfusion Injury
|
Sarcoma
|
Schizophrenia
|
Skin Diseases
|
Spastic Paraplegia 44, Autosomal Recessive
|
Stomach Neoplasms
|
Stomach Ulcer
|
Syndactyly
|
Syndactyly, Type 3
|
Tetralogy Of Fallot
|
Usher Syndrome, Type 2c
|
Abortion, Spontaneous
|
Vohwinkel Syndrome
|
Acute-Phase Reaction
|
Alagille Syndrome
|
Amphetamine-Related Disorders
|
Amyotrophic Lateral Sclerosis 1
|
Amyotrophic Lateral Sclerosis 9
|
Cardiac Arrhythmia
|
Arthritis, Juvenile
|
Astrocytoma
|
Atrial Fibrillation, Familial 1
|
Atrial Standstill
|
Bifid Nose
|
Bifid Nose With Or Without Anorectal And Renal Anomalies
|
Bone Diseases
|
Brain Neoplasms
|
Hepatocellular Carcinoma
|
Renal Cell Carcinoma
|
Cataract, Autosomal Dominant
|
Cataract Microcornea Syndrome
|
Cataract, Zonular Pulverulent 1
|
Cataract, Zonular Pulverulent 3
|
Cellulitis
|
Charcot-Marie-Tooth Disease, X-Linked, 1
|
Corneal Opacity
|
Coronary Aneurysm
|
Craniofacial Abnormalities
|
Deafness, Autosomal Dominant 2a
|