about
hereditary folate malabsorptiontranscobalamin II deficiencymultiple intestinal atresiaT-cell immunodeficiency, congenital alopecia, and nail dystrophyLaron syndrome with immunodeficiencyabsent thumb-short stature-immunodeficiency syndromeanhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndromeprimary immunodeficiency with natural-killer cell deficiency and adrenal insufficiencycombined immunodeficiency with faciooculoskeletal anomaliesfacial dysmorphism-immunodeficiency-livedo-short stature syndromepancytopenia due to IKZF1 mutationsDNA repair defect other than combined T-cell and B-cell immunodeficienciesImmuno-osseous dysplasiaimmunodeficiency due to absence of thymushyper-IgE syndromeautoinflammatory syndrome with pyogenic bacterial infection and amylopectinosisVici syndromeWiskott-Aldrich syndrome
P279
Q1609733-BEB100EA-70D1-4C25-B274-B5D485A3BB76Q18553496-F9EDE95F-F3AA-429F-BF35-087E00446941Q18554801-51E4A464-481D-4668-9ABE-AFCEA26DD43DQ28065574-034DB4D9-B649-4331-8C94-AA9FBD89E83EQ55782034-1548BA24-95FF-456D-A16C-1E4674E1E9F2Q55782350-6D4861E8-A2E7-4600-894D-D9D7020714FCQ55782438-749DC752-BC62-407F-BD3E-88B604FA2B43Q55783711-8CD0997C-F20A-40A6-8EFA-9752BDC3ECA8Q55783990-E416227E-5726-4255-92C1-56C597694069Q55784493-35477274-8760-4053-9256-5DA513961EB6Q55785025-9F0CC9DE-7941-4441-8A32-F9BFF5CB17ACQ55785655-E243B37A-8A4E-4283-B7FE-A86A936C078DQ55785657-83B0A7DE-C447-4562-8C1F-5114C650B3CFQ55787699-B12CED33-6D8D-4675-AD63-AF233917F50DQ55787700-76E0CEDE-2457-49E1-8094-72C567DDFF85Q56014071-dee93268-412f-d617-3b8b-ae03ab9f1f1dQ7925271-3E060D82-7EDA-40CD-A1C8-A10D2E4BC853Q953638-3ACFF3F5-D9A9-4E11-8D1D-E8A86FD75AF7
P279
description
human disease
@en
name
syndrome avec déficit immunitaire combiné
@fr
syndrome with combined immunodeficiency
@en
type
label
syndrome avec déficit immunitaire combiné
@fr
syndrome with combined immunodeficiency
@en
prefLabel
syndrome avec déficit immunitaire combiné
@fr
syndrome with combined immunodeficiency
@en
P1550
P2888
P5270
MONDO:0018035