Type chondrodysplasia. Medical search. Frequent questions

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Anatomy7

Growth Plate Cartilage Chondrocytes Microbodies Bone and Bones Peroxisomes Fibroblasts

Organisms2

Mice, Transgenic Mice, Mutant Strains

Diseases13

Chondrodysplasia Punctata Chondrodysplasia Punctata, Rhizomelic Osteochondrodysplasias Exostoses, Multiple Hereditary Dwarfism Bone Diseases, Developmental Peroxisomal Disorders Refsum Disease Zellweger Syndrome Limb Deformities, Congenital Achondroplasia Syndrome Fetal Diseases

Chemicals and Drugs14

Plasmalogens Collagen Type X Phytanic Acid Arylsulfatases Collagen Type XI Growth Differentiation Factor 5 Receptor, Parathyroid Hormone, Type 1 Acetyl-CoA C-Acetyltransferase Receptors, Parathyroid Hormone Collagen Matrilin Proteins Anion Transport Proteins Acyltransferases Parathyroid Hormone-Related Protein

Analytical, Diagnostic and Therapeutic Techniques and Equipment2

Pedigree DNA Mutational Analysis

Phenomena and Processes9

Bone Development Mutation Genes, Recessive Phenotype Homozygote Base Sequence Osteogenesis Point Mutation Heterozygote

Information Science2

Molecular Sequence Data Base Sequence

Named Groups1

Infant, Newborn

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Information Science Named Groups

Chondrodysplasia Punctata Chondrodysplasia Punctata, Rhizomelic Osteochondrodysplasias Exostoses, Multiple Hereditary Dwarfism Bone Diseases, Developmental Plasmalogens Growth Plate Collagen Type X Cartilage Phytanic Acid Peroxisomal Disorders Bone Development Refsum Disease Arylsulfatases Collagen Type XI Zellweger Syndrome Chondrocytes Growth Differentiation Factor 5 Receptor, Parathyroid Hormone, Type 1 Limb Deformities, Congenital Acetyl-CoA C-Acetyltransferase Achondroplasia Receptors, Parathyroid Hormone Collagen Microbodies Mutation Pedigree Genes, Recessive Matrilin Proteins Phenotype Bone and Bones Anion Transport Proteins Acyltransferases Homozygote Peroxisomes Parathyroid Hormone-Related Protein Syndrome Fetal Diseases Molecular Sequence Data Base Sequence Mice, Transgenic Osteogenesis DNA Mutational Analysis Fibroblasts Infant, Newborn Mice, Mutant Strains Point Mutation Heterozygote

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