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Abnormality of the nose
- Learning about Holoprosencephaly (HPE) (National Human Genome Research Institute)Craniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... National Human Genome Research Institute ... From the National Institutes of Health ... Holoprosencephaly ...
- Williams Syndrome (Genetic and Rare Diseases Information Center)Genetic Disorders/Specifics ... Genetic Disorders ... Developmental Disabilities/Specifics ... Developmental Disabilities ... Genetic and Rare Diseases Information Center ...
- Achondroplasia: About the Disease (Genetic and Rare Diseases Information Center)Dwarfism/Start Here ... Dwarfism ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and other information about ...
- Coffin Lowry Syndrome (National Institute of Neurological Disorders and Stroke)Facial Injuries and Disorders/Specifics ... Facial Injuries and Disorders ... Craniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... National Institute of ...
- Enlarged Vestibular Aqueducts and Childhood Hearing Loss (National Institute on Deafness and Other Communication Disorders)Hearing Problems in Children/Specifics ... Hearing Problems in Children ... Ear Disorders/Children ... Ear Disorders ... National Institute on Deafness and Other Communication ...
- Birth Disorders of the Brain and Spinal Cord (National Institute of Neurological Disorders and Stroke)Brain Diseases/Specifics ... Brain Diseases ... Neural Tube Defects/Specifics ... Neural Tube Defects ... Hydrocephalus/Specifics ... Hydrocephalus ... Spinal Cord Diseases/Specifics
- Alagille Syndrome (Genetic and Rare Diseases Information Center)Congenital Heart Defects/Genetics ... Congenital Heart Defects ... Bile Duct Diseases/Genetics ... Bile Duct Diseases ... Genetic and Rare Diseases Information Center ... From ...
- About Turner Syndrome (National Human Genome Research Institute)Turner Syndrome/Start Here ... Turner Syndrome ... National Human Genome Research Institute ... From the National Institutes of Health ... Turner syndrome is a chromosomal ...
- Campomelic dysplasia (Genetic and Rare Diseases Information Center)Find symptoms and other information about Campomelic dysplasia. ... Birth Defects/Specifics ... Birth Defects ... Bone Diseases/Children ... Bone Diseases ... Genetic and Rare ...
- About Duane Syndrome (National Human Genome Research Institute)Eye Movement Disorders/Genetics ... Eye Movement Disorders ... National Human Genome Research Institute ... From the National Institutes of Health ... Duane syndrome is a ...