Aplasia of the thymus

Symptom Information:

Symptom ID: HPO:0005359
Synonyms:
Thymic aplasia [Orphanet:36300]
Congenital hypoplasia of thymus (disorder) [Orphanet:36300]
Congenital absence of thymus (disorder) [Orphanet:36300]
Congenital absence of thymus [Orphanet:36300]
Congenital hypoplasia of thymus [Orphanet:36300]
Thymic aplasia/hypoplasia [Orphanet:36300]
Congenital thymus absence [Orphanet:36300]
Thymus hypoplasia [Orphanet:36300]
Congenital thymus absence [MedDRA:10048801]
Thymus hypoplasia [MedDRA:10052645]
Thymic aplasia [OMIM:Thymic aplasia]
Quality:
Cross references:
HPO:0000778 "Hypoplasia of the thymus" [Orphanet:36300]
Orphanet:36300 "Thymic aplasia/hypoplasia" [Orphanet:36300]
OMIM: "Thymic aplasia" [OMIM:Thymic aplasia]
UMLS:C0685894 "Congenital absence of thymus" [Orphanet:36300]
UMLS:C0685891 "Congenital hypoplasia of thymus" [Orphanet:36300]
Is a (Direct Parents):
MedDRA Thymus disorders
HPO         Aplasia/Hypoplasia of the thymus
Orphanet Abnormality of the lymphatic system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of the lymphatic system(HPO:0100763)
             Abnormality of the thymus(HPO:0000777)
                Aplasia/Hypoplasia of the thymus(HPO:0010515)
                   Aplasia of the thymus(HPO:0005359)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641)
       Thymus disorders(MedDRA:10043677)
          Aplasia of the thymus(HPO:0005359)
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
DIGEORGE SYNDROME (OMIM:188400)
Diabetic embryopathy (Orphanet:1926)
Reticular dysgenesis (Orphanet:33355)
Severe combined immunodeficiency due to DCLRE1C deficiency (Orphanet:275)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)