Abnormality of the thyroid gland

Symptom Information:

Symptom ID: HPO:0000820
Synonyms:
Thyroid abnormality [HPO:0000820]
Thyroid disease [HPO:0000820]
Thyroid gland anomaly [Orphanet:41120]
Thyroid disease [OMIM:Thyroid disease]
Thyroid anomalies [Orphanet:41120]
Thyroid disease (less common) [OMIM:Thyroid disease (less common)]
Quality:
Cross references:
Orphanet:41120 "Thyroid anomalies" [Orphanet:41120]
OMIM: "Thyroid disease" [OMIM:Thyroid disease]
OMIM: "Thyroid disease (less common)" [OMIM:Thyroid disease (less common)]
Is a (Direct Parents):
Orphanet Abnormality of the endocrine system
HPO         Abnormality of the endocrine system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          Abnormality of the thyroid gland(HPO:0000820)
MedDRA:
Database Frequency: 19 / 7739
Resource:

All diseases associated with this symptom:

Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
CHILD syndrome (Orphanet:139)
Choreoacanthocytosis (Orphanet:2388)
Congenital hypothyroidism (Orphanet:442)
Congenital hypothyroidism due to developmental anomaly (Orphanet:95711)
Cowden syndrome (Orphanet:201)
FACES syndrome (Orphanet:1969)
Flynn-Aird syndrome (Orphanet:2047)
Generalized resistance to thyroid hormone (Orphanet:3221)
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies (Orphanet:2234)
Methimazole embryofetopathy (Orphanet:1923)
Multiple endocrine neoplasia type 1 (Orphanet:652)
Odontotrichomelic syndrome (Orphanet:2723)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 (OMIM:609286)
Pallister-Hall syndrome (Orphanet:672)
Rabson-Mendenhall syndrome (Orphanet:769)
Thyrocerebrorenal syndrome (Orphanet:3327)
Thyroid ectopia (Orphanet:95712)
Weismann-Netter syndrome (Orphanet:3344)