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| Term | Nezelof syndrome | ID (Ontology) | DOID:2012 (Human Disease) |
| Definition | A T cell deficiency that results from the disfunction or underdevelopment of the thymus. | ||
| Also Known As | "Nezelof's syndrome" ; "T-cell immunodeficiency with thymic aplasia" ; "thymic aplasia" (for all, see Synonyms field below) | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal recessive disease___ primary immunodeficiency disease | |__T cell deficiency_____________| Nezelof syndrome 1 rec. |
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Relationships
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| Is a |
autosomal recessive disease T cell deficiency |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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ICD10CM:D81.4 ICD9CM:279.13 MIM:242700 ORDO:83471 SNOMEDCT_US_2023_03_01:55602000 UMLS_CUI:C0152094 |
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