CDC/NIH Web Information Database
Primary Immune Deficiency Diseases
Last data update: Dec 04, 2023. (Total: 8775 Documents)
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Gene therapy restores immunity in infants with rare immunodeficiency disease
NIH News, April 17, 2019 
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Check out genetic conditions and tests associated with Wiskott-Aldrich Syndrome
from the NIH Genetic Testing Registry
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What is Wiskott-Aldrich syndrome?
From the NIH Genetics Home Reference
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Bloom Syndrome MedGen Information
from the National Library of Medicine
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check out genetic conditions and tests associated with Bloom Syndrome
From the NIH Genetic Testing Registry
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Bloom Syndrome: Gene Reviews
MM Sanz et al. 2013
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Antiphospholipid Antibody Syndrome
From NHLBI health topic site
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Hemophilia
From NHLBI health topic site
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Lymphocytopenia
From NHLBI health topic site
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CHARGE syndrome
From NCATS Genetic and Rare Diseases Information Center
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Hypohidrotic ectodermal dysplasia
From NCATS Genetic and Rare Diseases Information Center
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Facial ectodermal dysplasia
From NCATS Genetic and Rare Diseases Information Center
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Severe congenital neutropenia autosomal recessive 3
From NCATS Genetic and Rare Diseases Information Center
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Blau syndrome
From NCATS Genetic and Rare Diseases Information Center
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Jacobsen syndrome
From NCATS Genetic and Rare Diseases Information Center
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Osteopetrosis autosomal dominant type 2
From NCATS Genetic and Rare Diseases Information Center
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ZAP-70 deficiency
From NCATS Genetic and Rare Diseases Information Center
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Vici syndrome
From NCATS Genetic and Rare Diseases Information Center
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Aicardi-Goutieres syndrome
From NCATS Genetic and Rare Diseases Information Center
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Bloom syndrome
From NCATS Genetic and Rare Diseases Information Center
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X-linked agammaglobulinemia
From NCATS Genetic and Rare Diseases Information Center
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Cerebellar ataxia ectodermal dysplasia
From NCATS Genetic and Rare Diseases Information Center
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Arthrogryposis, ectodermal dysplasia, cleft lip/palate, and developmental delay
From NCATS Genetic and Rare Diseases Information Center
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Arthrogryposis and ectodermal dysplasia
From NCATS Genetic and Rare Diseases Information Center
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Dyskeratosis congenita X-linked
From NCATS Genetic and Rare Diseases Information Center
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Ectodermal dysplasia alopecia preaxial polydactyly
From NCATS Genetic and Rare Diseases Information Center
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Ectodermal dysplasia arthrogryposis diabetes mellitus
From NCATS Genetic and Rare Diseases Information Center
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Ectodermal dysplasia Bartalos type
From NCATS Genetic and Rare Diseases Information Center
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Ectodermal dysplasia Berlin type
From NCATS Genetic and Rare Diseases Information Center
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Ectodermal dysplasia blindness
From NCATS Genetic and Rare Diseases Information Center
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