Genetic disorders pathway noonan syndrome. Medical search. Frequent questions

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Anatomy1

Diseases18

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

Chemicals and Drugs5

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment3

Facies Diagnostic Techniques, Endocrine DNA Mutational Analysis

Phenomena and Processes6

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

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

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

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