Neurofibromin genetic noonan syndrome. Medical search. Frequent questions

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Anatomy1

Diseases18

Noonan Syndrome LEOPARD Syndrome Neurofibromatosis 1 Syndrome Costello Syndrome Facies Loose Anagen Hair Syndrome Pulmonary Valve Stenosis Abnormalities, Multiple Failure to Thrive Cherubism Skin Abnormalities Craniofacial Abnormalities Ectodermal Dysplasia Bezoars Heart Defects, Congenital Leukemia, Myelomonocytic, Juvenile Cardiomyopathy, Hypertrophic

Chemicals and Drugs7

Neurofibromin 1 Protein Tyrosine Phosphatase, Non-Receptor Type 11 SOS1 Protein ras Proteins Protein Tyrosine Phosphatases ras GTPase-Activating Proteins Intracellular Signaling Peptides and Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment2

Facies Diagnostic Techniques, Endocrine

Phenomena and Processes5

Genes, Neurofibromatosis 1 Mutation Sexual Development Germ-Line Mutation Phenotype

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes

Noonan Syndrome Neurofibromin 1 LEOPARD Syndrome Protein Tyrosine Phosphatase, Non-Receptor Type 11 SOS1 Protein Genes, Neurofibromatosis 1 Neurofibromatosis 1 Syndrome Costello Syndrome Facies Loose Anagen Hair Syndrome Pulmonary Valve Stenosis Eyebrows Abnormalities, Multiple Failure to Thrive ras Proteins Protein Tyrosine Phosphatases Cherubism Skin Abnormalities Craniofacial Abnormalities Mutation Ectodermal Dysplasia Sexual Development Bezoars ras GTPase-Activating Proteins Heart Defects, Congenital Leukemia, Myelomonocytic, Juvenile Germ-Line Mutation Diagnostic Techniques, Endocrine Cardiomyopathy, Hypertrophic Intracellular Signaling Peptides and Proteins Phenotype

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