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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
hypothyroidism +     
mucinoses +     
Bamforth-Lazarus syndrome  
BRANCHIAL ARCH ABNORMALITIES, CHOANAL ATRESIA, ATHELIA, HEARING LOSS, AND HYPOTHYROIDISM SYNDROME  
congenital hypothyroidism +   
follicular mucinosis 
Hypohidrotic Ectodermal Dysplasia with Hypothyroidism and Ciliary Dyskinesia 
IGSF1 deficiency syndrome  
iodine hypothyroidism 
Johanson-Blizzard syndrome  
Jung Wolff Back Stahl Syndrome 
Li-Campeau Syndrome  
mucopolysaccharidosis +   
myxedema 
A condition characterized by a dry, waxy type of swelling (EDEMA) with abnormal deposits of MUCOPOLYSACCHARIDES in the SKIN and other tissues. It is caused by a deficiency of THYROID HORMONES. The skin becomes puffy around the eyes and on the cheeks. The face is dull and expressionless with thickened nose and lips.
postsurgical hypothyroidism 
scleredema adultorum 
Scleromyxedema  
thyroid hormone resistance syndrome +   
Thyrotropin-Releasing Hormone Deficiency  
Zadik Barak Levin Syndrome 

Synonyms
Exact Synonyms: myxedemas
Primary IDs: MESH:D009230
Alternate IDs: OMIM:255900
Xrefs: EFO:1001055 ;   NCI:C34834
Definition Sources: MESH:D009230

paths to the root