Hypoplasia of the thymus

Symptom Information:

Symptom ID: HPO:0000778
Synonyms:
Thymus hypoplasia [HPO:0000778]
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]
Thymus hypoplasia [OMIM:Thymus hypoplasia]
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:0005359 "Aplasia of the thymus" [Orphanet:36300]
Orphanet:36300 "Thymic aplasia/hypoplasia" [Orphanet:36300]
OMIM: "Thymus hypoplasia" [OMIM:Thymus hypoplasia]
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):
Orphanet Abnormality of the lymphatic system
MedDRA Thymus disorders
HPO         Aplasia/Hypoplasia of the thymus
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)
                   Hypoplasia of the thymus(HPO:0000778)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Spleen, lymphatic and reticuloendothelial system disorders(MedDRA:10041641)
       Thymus disorders(MedDRA:10043677)
          Hypoplasia of the thymus(HPO:0000778)
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

ATAXIA-TELANGIECTASIA (OMIM:208900)
ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3 (OMIM:170995)
Ataxia-telangiectasia (Orphanet:100)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
DIGEORGE SYNDROME (OMIM:188400)
Leprechaunism (Orphanet:508)
Multiple intestinal atresia (Orphanet:2300)
Omenn syndrome (Orphanet:39041)
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) (OMIM:214110)
Reticular dysgenesis (Orphanet:33355)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Short-limb skeletal dysplasia with severe combined immunodeficiency (Orphanet:935)
T-B+ severe combined immunodeficiency due to gamma chain deficiency (Orphanet:276)