Primary hypothyroidism
Symptom Information:
Symptom ID: | HPO:0000832 | ||||
Synonyms: |
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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) Abnormality of thyroid physiology(HPO:0002926) Hypothyroidism(HPO:0000821) Primary hypothyroidism(HPO:0000832) MedDRA: Endocrine disorders(MedDRA:10014698) Thyroid gland disorders(MedDRA:10043739) Thyroid hypofunction disorders(MedDRA:10043741) Primary hypothyroidism(HPO:0000832) |
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Database Frequency: | 4 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Ectodermal dysplasia - intellectual deficit - central nervous system malformation | (Orphanet:1812) |
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia | (Orphanet:1882) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |