Hypothyroidism
Symptom Information:
Symptom ID: | HPO:0000821 | ||||||||||||||||||||||||||||
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 physiology(HPO:0002926) Hypothyroidism(HPO:0000821) MedDRA: Endocrine disorders(MedDRA:10014698) Thyroid gland disorders(MedDRA:10043739) Thyroid hypofunction disorders(MedDRA:10043741) Hypothyroidism(HPO:0000821) |
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Database Frequency: | 141 / 7739 | ||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
17p11.2 microduplication syndrome | (Orphanet:1713) |
19p13.12 microdeletion syndrome | (Orphanet:254346) |
1p36 deletion syndrome | (Orphanet:1606) |
22q11.2 deletion syndrome | (Orphanet:567) |
46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency | (Orphanet:752) |
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET | (OMIM:615952) |
Aceruloplasminemia | (Orphanet:48818) |
Acetazolamide-responsive myotonia | (Orphanet:99736) |
Adiposis dolorosa | (Orphanet:36397) |
Albright hereditary osteodystrophy | (Orphanet:665) |
Alexander disease | (Orphanet:58) |
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
Alström syndrome | (Orphanet:64) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Ascher syndrome | (Orphanet:1253) |
Athyreosis | (Orphanet:95713) |
Autoimmune polyendocrinopathy type 2 | (Orphanet:3143) |
Autosomal recessive cutis laxa type 1 | (Orphanet:90349) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Bamforth syndrome | (Orphanet:1226) |
Bangstad syndrome | (Orphanet:1227) |
Bardet-Biedl syndrome 12 | (OMIM:615989) |
Beckwith-Wiedemann syndrome | (Orphanet:116) |
Beta-thalassemia major | (Orphanet:231214) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
Blepharophimosis-intellectual deficit syndrome, SBBYS type | (Orphanet:3047) |
CHARGE syndrome | (Orphanet:138) |
COWDEN SYNDROME 5 | (OMIM:615108) |
COWDEN SYNDROME 6 | (OMIM:615109) |
Castleman disease | (Orphanet:160) |
Cenani-Lenz syndrome | (Orphanet:3258) |
Central congenital hypothyroidism | (Orphanet:226298) |
Central precocious puberty | (Orphanet:759) |
Congenital atransferrinemia | (Orphanet:1195) |
Congenital hypothyroidism | (Orphanet:442) |
Congenital hypothyroidism due to developmental anomaly | (Orphanet:95711) |
Congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies | (Orphanet:95715) |
Congenital nephrotic syndrome, Finnish type | (Orphanet:839) |
Cowden syndrome | (Orphanet:201) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
Cutis laxa | (Orphanet:209) |
Cutis marmorata telangiectatica congenita | (Orphanet:1556) |
Cystinosis | (Orphanet:213) |
DIGEORGE SYNDROME | (OMIM:188400) |
Dahlberg-Borer-Newcomer syndrome | (Orphanet:1563) |
Deafness - intellectual deficit, Martin-Probst type | (Orphanet:85321) |
Down syndrome | (Orphanet:870) |
Ectodermal dysplasia - intellectual deficit - central nervous system malformation | (Orphanet:1812) |
Fabry disease | (Orphanet:324) |
Familial thyroid dyshormonogenesis | (Orphanet:95716) |
Fetal iodine syndrome | (Orphanet:1910) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
Fucosidosis | (Orphanet:349) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hawkinsinuria | (Orphanet:2118) |
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia | (Orphanet:1882) |
Hypothyroidism due to TSH receptor mutations | (Orphanet:90673) |
Hypothyroidism due to deficient transcription factors involved in pituitary development or function | (Orphanet:226307) |
IMMUNODEFICIENCY 31C | (OMIM:614162) |
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY | (OMIM:614700) |
Idiopathic congenital hypothyroidism | (Orphanet:95717) |
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | (Orphanet:37042) |
Immunodeficiency due to CD25 deficiency | (Orphanet:169100) |
Infantile axonal neuropathy | (Orphanet:2679) |
Isolated anterior cervical hypertrichosis | (Orphanet:3387) |
Isolated growth hormone deficiency type III | (Orphanet:231692) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
Jung-Wolff-Back-Stahl syndrome | (Orphanet:2321) |
Koolen-De Vries syndrome | (Orphanet:96169) |
LIG4 syndrome | (Orphanet:99812) |
Lhermitte-Duclos disease | (Orphanet:65285) |
MELAS | (Orphanet:550) |
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 | (OMIM:614114) |
MYXEDEMA | (OMIM:255900) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
Methimazole embryofetopathy | (Orphanet:1923) |
Microcephaly - seizures - intellectual deficit - heart disease | (Orphanet:2519) |
Microphthalmia with brain and digit anomalies | (Orphanet:139471) |
Monosomy 18p | (Orphanet:1598) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Mullerian duct anomalies - limb anomalies | (Orphanet:2491) |
Muscular pseudohypertrophy - hypothyroidism | (Orphanet:2349) |
NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET | (OMIM:616263) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Obesity - colitis - hypothyroidism - cardiac hypertrophy - developmental delay | (Orphanet:88643) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Omenn syndrome | (Orphanet:39041) |
PGM1-CDG | (Orphanet:319646) |
PHACE syndrome | (Orphanet:42775) |
PITUITARY DWARFISM WITH LARGE SELLA TURCICA | (OMIM:262710) |
PITUITARY HORMONE DEFICIENCY, COMBINED, 1 | (OMIM:613038) |
PITUITARY HORMONE DEFICIENCY, COMBINED, 2 | (OMIM:262600) |
PMM2-CDG | (Orphanet:79318) |
POEMS syndrome | (Orphanet:2905) |
PREMATURE OVARIAN FAILURE 10 | (OMIM:612885) |
Panhypopituitarism | (Orphanet:90695) |
Pendred syndrome | (Orphanet:705) |
Peripheral hypothyroidism | (Orphanet:226310) |
Peripheral resistance to thyroid hormones | (Orphanet:97927) |
Permanent congenital hypothyroidism | (Orphanet:226292) |
Pituitary stalk interruption syndrome | (Orphanet:95496) |
Primary congenital hypothyroidism | (Orphanet:226295) |
Primary congenital hypothyroidism without thyroid developmental anomaly | (Orphanet:95714) |
Proteus-like syndrome | (Orphanet:2969) |
Proximal myotonic myopathy | (Orphanet:606) |
Pseudohypoparathyroidism type 1A | (Orphanet:79443) |
Pseudohypoparathyroidism type 1C | (Orphanet:79444) |
Pseudoxanthoma elasticum | (Orphanet:758) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Resistance to thyrotropin-releasing hormone syndrome | (Orphanet:99832) |
Retinohepatoendocrinologic syndrome | (Orphanet:3087) |
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION | (OMIM:607944) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Short stature - craniofacial anomalies - genital hypoplasia | (Orphanet:2994) |
Short stature - pituitary and cerebellar defects - small sella turcica | (Orphanet:85442) |
Smith-Magenis syndrome | (Orphanet:819) |
Solitary median maxillary central incisor syndrome | (Orphanet:2286) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
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 DYSHORMONOGENESIS 6 | (OMIM:607200) |
TUBEROUS SCLEROSIS 1 | (OMIM:191100) |
TUBEROUS SCLEROSIS 2 | (OMIM:613254) |
Thyroid ectopia | (Orphanet:95712) |
Thyroid hemiagenesis | (Orphanet:95719) |
Thyroid hypoplasia | (Orphanet:95720) |
Timothy syndrome | (Orphanet:65283) |
Townes-Brocks syndrome | (Orphanet:857) |
Transient congenital hypothyroidism | (Orphanet:178045) |
Tuberous sclerosis | (Orphanet:805) |
Whipple disease | (Orphanet:3452) |
Williams syndrome | (Orphanet:904) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
Wolfram syndrome 1 | (OMIM:222300) |
X-linked central congenital hypothyroidism with late-onset testicular enlargement | (Orphanet:329235) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |