MCID: CNG543
MIFTS: 12

Congenital Hypothyroidism Due to Transplacental Passage of Tsh-Binding Inhibitory Antibodies

Categories: Endocrine diseases, Immune diseases, Metabolic diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Congenital Hypothyroidism Due to Transplacental Passage of...

MalaCards integrated aliases for Congenital Hypothyroidism Due to Transplacental Passage of Tsh-Binding Inhibitory Antibodies:

Name: Congenital Hypothyroidism Due to Transplacental Passage of Tsh-Binding Inhibitory Antibodies 58

Characteristics:

Orphanet epidemiological data:

58

Classifications:

Orphanet: 58  
Rare endocrine diseases


Summaries for Congenital Hypothyroidism Due to Transplacental Passage of...

MalaCards based summary : Congenital Hypothyroidism Due to Transplacental Passage of Tsh-Binding Inhibitory Antibodies Affiliated tissues include thyroid, and related phenotypes are constipation and hypothyroidism

Related Diseases for Congenital Hypothyroidism Due to Transplacental Passage of...

Symptoms & Phenotypes for Congenital Hypothyroidism Due to Transplacental Passage of...

Human phenotypes related to Congenital Hypothyroidism Due to Transplacental Passage of Tsh-Binding Inhibitory Antibodies:

58 31 (show all 13)
# Description HPO Frequency Orphanet Frequency HPO Source Accession
1 constipation 58 31 hallmark (90%) Very frequent (99-80%) HP:0002019
2 hypothyroidism 58 31 hallmark (90%) Very frequent (99-80%) HP:0000821
3 muscular hypotonia 58 31 hallmark (90%) Very frequent (99-80%) HP:0001252
4 macroglossia 58 31 hallmark (90%) Very frequent (99-80%) HP:0000158
5 coarse facial features 58 31 hallmark (90%) Very frequent (99-80%) HP:0000280
6 global developmental delay 58 31 hallmark (90%) Very frequent (99-80%) HP:0001263
7 umbilical hernia 58 31 hallmark (90%) Very frequent (99-80%) HP:0001537
8 growth delay 58 31 hallmark (90%) Very frequent (99-80%) HP:0001510
9 jaundice 58 31 hallmark (90%) Very frequent (99-80%) HP:0000952
10 abnormality of the immune system 58 31 hallmark (90%) Very frequent (99-80%) HP:0002715
11 large fontanelles 58 31 hallmark (90%) Very frequent (99-80%) HP:0000239
12 abdominal distention 58 31 hallmark (90%) Very frequent (99-80%) HP:0003270
13 hypersomnia 58 31 hallmark (90%) Very frequent (99-80%) HP:0100786

Drugs & Therapeutics for Congenital Hypothyroidism Due to Transplacental Passage of...

Search Clinical Trials , NIH Clinical Center for Congenital Hypothyroidism Due to Transplacental Passage of Tsh-Binding Inhibitory Antibodies

Genetic Tests for Congenital Hypothyroidism Due to Transplacental Passage of...

Anatomical Context for Congenital Hypothyroidism Due to Transplacental Passage of...

MalaCards organs/tissues related to Congenital Hypothyroidism Due to Transplacental Passage of Tsh-Binding Inhibitory Antibodies:

40
Thyroid

Publications for Congenital Hypothyroidism Due to Transplacental Passage of...

Variations for Congenital Hypothyroidism Due to Transplacental Passage of...

Expression for Congenital Hypothyroidism Due to Transplacental Passage of...

Search GEO for disease gene expression data for Congenital Hypothyroidism Due to Transplacental Passage of Tsh-Binding Inhibitory Antibodies.

Pathways for Congenital Hypothyroidism Due to Transplacental Passage of...

GO Terms for Congenital Hypothyroidism Due to Transplacental Passage of...

Sources for Congenital Hypothyroidism Due to Transplacental Passage of...

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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