ORPHA:238696

Transient congenital hypothyroidism due to maternal factor

Type: Category
Group: Group of disorders
Status: active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Transient congenital hypothyroidism due to maternal factor
fr	Hypothyroïdie congénitale transitoire de cause maternelle
de	Hypothyreose, kongenitale transiente, durch maternalen Faktor
es	Hipotiroidimo congénito transitorio por causa materna
it	Ipotiroidismo congenito transitorio di origine materna
nl	Tijdelijke congenitale hypothyreoïdie als gevolg van maternale factor
pt	Hipotiroidismo transitório congénito por fator materno
pl	Przejściowa wrodzona niedoczynność tarczycy z powodu czynnika matczynego
cs	Tranzientní vrozená hypotyreóza způsobená faktorem ze strany matky
uk	Транзиторний вроджений гіпотиреоз через материнський фактор
zh	妊娠期因素所致短暂性先天性甲状腺功能减退
tr	Maternal faktöre bağlı geçici doğumsal hipotiroidi

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	Validation
MONDO	0016555	E	validated
MONDO	16555	E	validated
UMLS	C5680929	E	validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:97978Rare endocrine disease

Parents in the classifications (1):

ORPHA:178045Transient congenital hypothyroidism
rare endocrine diseases

Children (3):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/238696
This record as JSON: /data/d/238696.json