Abnormality of the tonsils

Symptom Information:

Symptom ID: HPO:0100765
Synonyms:
Tonsil anomaly [Orphanet:26080]
Tonsil anomaly/hypertrophy/adenoiditis [Orphanet:26080]
Tonsillar inflammation [MedDRA:10065169]
Adenoiditis [Orphanet:26080]
Adenoiditis (disorder) [Orphanet:26080]
Tonsillitis (disorder) [Orphanet:26080]
Inflamed tonsils (finding) [Orphanet:26080]
Tonsillitis [Orphanet:26080]
Tonsillar hypertrophy [MedDRA:10044003]
Tonsil hypertrophy [Orphanet:26080]
Hypertrophy of tonsils (disorder) [Orphanet:26080]
Hypertrophy of tonsils [Orphanet:26080]
Tonsillar hypertrophy [OMIM:Tonsillar hypertrophy]
Quality:
Cross references:
Orphanet:26080 "Tonsil anomaly/hypertrophy/adenoiditis" [Orphanet:26080]
OMIM: "Tonsillar hypertrophy" [OMIM:Tonsillar hypertrophy]
UMLS:C0559684 "Inflamed tonsils (finding)" [Orphanet:26080]
UMLS:C0040425 "Tonsillitis" [Orphanet:26080]
UMLS:C0001427 "Adenoiditis" [Orphanet:26080]
UMLS:C0272386 "Hypertrophy of tonsils" [Orphanet:26080]
Is a (Direct Parents):
HPO         Abnormality of the lymphatic system
Orphanet Tonsillitis
HPO         Abnormality of lingual tonsil
Orphanet Structural anomalies of the digestive tract
HPO         Abnormality of nasopharyngeal adenoids
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 tonsils(HPO:0100765)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Isolated agammaglobulinemia (Orphanet:229717)
Lung fibrosis - immunodeficiency - 46,XX gonadal dysgenesis (Orphanet:137631)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Scheie syndrome (Orphanet:93474)
Severe combined immunodeficiency (Orphanet:183660)
X-linked agammaglobulinemia (Orphanet:47)
X-linked hyper-IgM syndrome (Orphanet:101088)