Ectodermal Dysplasia
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Last Posted: Jan 01, 2011
- Congenital ectodermal dysplasia with hearing loss
From NCATS Genetic and Rare Diseases Information Center - Ectodermal dysplasia
From NCATS Genetic and Rare Diseases Information Center - Ectodermal dysplasia Bartalos type
From NCATS Genetic and Rare Diseases Information Center - Ectodermal dysplasia Berlin type
From NCATS Genetic and Rare Diseases Information Center - Ectodermal dysplasia blindness
From NCATS Genetic and Rare Diseases Information Center - Ectodermal dysplasia intellectual disability CNS malformation
From NCATS Genetic and Rare Diseases Information Center - Ectodermal dysplasia Margarita type
From NCATS Genetic and Rare Diseases Information Center - Ectodermal dysplasia neurosensory deafness
From NCATS Genetic and Rare Diseases Information Center - Ectodermal dysplasia skin fragility syndrome
From NCATS Genetic and Rare Diseases Information Center - Ectodermal dysplasia trichoodontoonychial type
From NCATS Genetic and Rare Diseases Information Center - Ectodermal dysplasia with natal teeth Turnpenny type
From NCATS Genetic and Rare Diseases Information Center - Ectodermal dysplasia, hidrotic, Christianson-Fourie type
From NCATS Genetic and Rare Diseases Information Center - Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features
From NCATS Genetic and Rare Diseases Information Center - Hypohidrotic ectodermal dysplasia autosomal dominant
From NCATS Genetic and Rare Diseases Information Center - Hypohidrotic ectodermal dysplasia autosomal recessive
From NCATS Genetic and Rare Diseases Information Center - Hypohidrotic ectodermal dysplasia with hypothyroidism and ciliary dyskinesia
From NCATS Genetic and Rare Diseases Information Center - Hypohidrotic ectodermal dysplasia with immune deficiency
From NCATS Genetic and Rare Diseases Information Center - Immunodeficiency without anhidrotic ectodermal dysplasia
From NCATS Genetic and Rare Diseases Information Center - Syndactyly ectodermal dysplasia cleft lip palate hand foot
From NCATS Genetic and Rare Diseases Information Center - Tetraamelia with ectodermal dysplasia and lacrimal duct abnormalities
From NCATS Genetic and Rare Diseases Information Center
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Neurological Disorders (ND) PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to neurological disorders....more
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Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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