Goiter

Symptom Information:

Symptom ID: HPO:0000853
Synonyms:
Goitre [HPO:0000853]
Goiter (disorder) [Orphanet:41150]
GOITRE [HPO:0000853]
Goiter [Orphanet:41150]
Goiter [OMIM:Goiter]
Goitre [Orphanet:41150]
Goitre [MedDRA:10018498]
Dyshormonogenic goiter [MedDRA:10018498]
Dyshormonogenic goitre [MedDRA:10018498]
Enlarged thyroid [MedDRA:10018498]
Goiter [MedDRA:10018498]
Goiter diffuse [MedDRA:10018498]
Goiter nodular [MedDRA:10018498]
Goiter, specified as simple [MedDRA:10018498]
Goiter, unspecified [MedDRA:10018498]
Goitre nontoxic [MedDRA:10018498]
Goitre, specified as simple [MedDRA:10018498]
Goitre, unspecified [MedDRA:10018498]
Non-toxic multinodular goitre [MedDRA:10018498]
Non-toxic nodular goitre [MedDRA:10018498]
Non-toxic uninodular goitre [MedDRA:10018498]
Nontoxic goiter [MedDRA:10018498]
Nontoxic goitre [MedDRA:10018498]
Nontoxic multinodular goiter [MedDRA:10018498]
Nontoxic multinodular goitre [MedDRA:10018498]
Nontoxic nodular goiter [MedDRA:10018498]
Nontoxic nodular goitre [MedDRA:10018498]
Nontoxic nodular goitre, unspecified [MedDRA:10018498]
Nontoxic uninodular goiter [MedDRA:10018498]
Nontoxic uninodular goitre [MedDRA:10018498]
Simple and unspecified goiter [MedDRA:10018498]
Simple and unspecified goitre [MedDRA:10018498]
Simple goitre [MedDRA:10018498]
Thyroid enlarged [MedDRA:10018498]
Unspecified nontoxic nodular goiter [MedDRA:10018498]
Unspecified nontoxic nodular goitre [MedDRA:10018498]
Adenomatous goitre [MedDRA:10018498]
Thyroid hyperplasia [MedDRA:10018498]
Adenomatous goiter [MedDRA:10018498]
Goitre diffuse [MedDRA:10018498]
Goitre nodular [MedDRA:10018498]
Euthyroid goiter [MedDRA:10018498]
Euthyroid goitre [MedDRA:10018498]
Iodine deficiency goiter [MedDRA:10018498]
Iodine deficiency goitre [MedDRA:10018498]
Parenchymatous goitre [MedDRA:10018498]
Parenchymatous goiter [MedDRA:10018498]
Thyromegaly [MedDRA:10018498]
Asymmetric thyroid [MedDRA:10018498]
Endemic goiter [MedDRA:10018498]
Endemic goitre [MedDRA:10018498]
Transient thyroid enlargement [MedDRA:10018498]
Plunging goitre [MedDRA:10018498]
Plunging goiter [MedDRA:10018498]
Simple goiter [MedDRA:10018498]
Goiter (not always present) [OMIM:Goiter (not always present)]
Nontoxic goiter [OMIM:Nontoxic goiter]
Quality:
Cross references:
Orphanet:41150 "Goiter" [Orphanet:41150]
OMIM: "Goiter" [OMIM:Goiter]
OMIM: "Goiter (not always present)" [OMIM:Goiter (not always present)]
OMIM: "Nontoxic goiter" [OMIM:Nontoxic goiter]
UMLS:C0018021 "GOITRE" [HPO:0000853]
UMLS:C0018021 "Goiter" [Orphanet:41150]
Is a (Direct Parents):
MedDRA Thyroid disorders NEC
Orphanet Abnormality of the thyroid gland
HPO         Abnormality of thyroid morphology
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)
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)