Abnormality of the thyroid gland
Symptom Information:
Symptom ID: | HPO:0000820 | ||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |