Goiter
Symptom Information:
Symptom ID: | HPO:0000853 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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) Abnormality of thyroid morphology(HPO:0011772) Goiter(HPO:0000853) MedDRA: Endocrine disorders(MedDRA:10014698) Thyroid gland disorders(MedDRA:10043739) Thyroid disorders NEC(MedDRA:10043712) Goiter(HPO:0000853) |
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Database Frequency: | 39 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Albright hereditary osteodystrophy | (Orphanet:665) |
Ascher syndrome | (Orphanet:1253) |
Bangstad syndrome | (Orphanet:1227) |
COWDEN SYNDROME 5 | (OMIM:615108) |
COWDEN SYNDROME 6 | (OMIM:615109) |
Cogan syndrome | (Orphanet:1467) |
Congenital hypothyroidism | (Orphanet:442) |
Cowden syndrome | (Orphanet:201) |
DEIODINASE, IODOTHYRONINE, TYPE I | (OMIM:147892) |
Familial hyperthyroidism due to mutations in TSH receptor | (Orphanet:424) |
Familial thyroid dyshormonogenesis | (Orphanet:95716) |
Fetal iodine syndrome | (Orphanet:1910) |
GRAVES DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:275000) |
Generalized resistance to thyroid hormone | (Orphanet:3221) |
Glutaric acidemia type 3 | (Orphanet:35706) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
Lhermitte-Duclos disease | (Orphanet:65285) |
MELAS | (Orphanet:550) |
Maffucci syndrome | (Orphanet:163634) |
McCune-Albright syndrome | (Orphanet:562) |
Multinodular goiter - cystic kidney - polydactyly | (Orphanet:2091) |
Pendred syndrome | (Orphanet:705) |
Permanent congenital hypothyroidism | (Orphanet:226292) |
Proteus-like syndrome | (Orphanet:2969) |
THYROID DYSHORMONOGENESIS 1 | (OMIM:274400) |
THYROID DYSHORMONOGENESIS 2A | (OMIM:274500) |
THYROID DYSHORMONOGENESIS 3 | (OMIM:274700) |
THYROID DYSHORMONOGENESIS 4 | (OMIM:274800) |
THYROID DYSHORMONOGENESIS 5 | (OMIM:274900) |
THYROID HORMONE PLASMA MEMBRANE TRANSPORT DEFECT | (OMIM:188560) |
THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT | (OMIM:188570) |
THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL RECESSIVE | (OMIM:274300) |
THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1 | (OMIM:188580) |
THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2 | (OMIM:613239) |
Thyrocerebrorenal syndrome | (Orphanet:3327) |
Thyroid ectopia | (Orphanet:95712) |
Thyroid hemiagenesis | (Orphanet:95719) |
Thyrotoxic periodic paralysis | (Orphanet:79102) |
Transient congenital hypothyroidism | (Orphanet:178045) |