Central hypothyroidism
Symptom Information:
Symptom ID: | HPO:0011787 | ||
Synonyms: |
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Quality: | |||
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) Abnormality of thyroid physiology(HPO:0002926) Hypothyroidism(HPO:0000821) Central hypothyroidism(HPO:0011787) MedDRA: |
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Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Microcephalic primordial dwarfism, Dauber type | (Orphanet:319675) |
POLYENDOCRINE-POLYNEUROPATHY SYNDROME | (OMIM:616113) |
Wolfram syndrome 1 | (OMIM:222300) |
X-linked central congenital hypothyroidism with late-onset testicular enlargement | (Orphanet:329235) |