CDC/NIH Web Information Database
Primary Immune Deficiency Diseases
Last data update: Apr 16, 2024. (Total: 8777 Documents)
CDC/NIH Web Information |
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Gene therapy restores immunity in infants with rare immunodeficiency disease
NIH News, April 17, 2019 |
Check out genetic conditions and tests associated with Wiskott-Aldrich Syndrome
from the NIH Genetic Testing Registry |
What is Wiskott-Aldrich syndrome?
From the NIH Genetics Home Reference |
Bloom Syndrome MedGen Information
from the National Library of Medicine |
check out genetic conditions and tests associated with Bloom Syndrome
From the NIH Genetic Testing Registry |
Bloom Syndrome: Gene Reviews
MM Sanz et al. 2013 |
Antiphospholipid Antibody Syndrome
From NHLBI health topic site |
Hemophilia
From NHLBI health topic site |
Lymphocytopenia
From NHLBI health topic site |
CHARGE syndrome
From NCATS Genetic and Rare Diseases Information Center |
Hypohidrotic ectodermal dysplasia
From NCATS Genetic and Rare Diseases Information Center |
Facial ectodermal dysplasia
From NCATS Genetic and Rare Diseases Information Center |
Severe congenital neutropenia autosomal recessive 3
From NCATS Genetic and Rare Diseases Information Center |
Blau syndrome
From NCATS Genetic and Rare Diseases Information Center |
Jacobsen syndrome
From NCATS Genetic and Rare Diseases Information Center |
Osteopetrosis autosomal dominant type 2
From NCATS Genetic and Rare Diseases Information Center |
ZAP-70 deficiency
From NCATS Genetic and Rare Diseases Information Center |
Vici syndrome
From NCATS Genetic and Rare Diseases Information Center |
Aicardi-Goutieres syndrome
From NCATS Genetic and Rare Diseases Information Center |
Bloom syndrome
From NCATS Genetic and Rare Diseases Information Center |
X-linked agammaglobulinemia
From NCATS Genetic and Rare Diseases Information Center |
Cerebellar ataxia ectodermal dysplasia
From NCATS Genetic and Rare Diseases Information Center |
Arthrogryposis, ectodermal dysplasia, cleft lip/palate, and developmental delay
From NCATS Genetic and Rare Diseases Information Center |
Arthrogryposis and ectodermal dysplasia
From NCATS Genetic and Rare Diseases Information Center |
Dyskeratosis congenita X-linked
From NCATS Genetic and Rare Diseases Information Center |
Ectodermal dysplasia alopecia preaxial polydactyly
From NCATS Genetic and Rare Diseases Information Center |
Ectodermal dysplasia arthrogryposis diabetes mellitus
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 |