MCID: CNG591
MIFTS: 7

Congenital Hypothyroidism Due to Developmental Anomaly

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

Aliases & Classifications for Congenital Hypothyroidism Due to Developmental Anomaly

MalaCards integrated aliases for Congenital Hypothyroidism Due to Developmental Anomaly:

Name: Congenital Hypothyroidism Due to Developmental Anomaly 58
Primary Congenital Hypothyroidism Due to Developmental Anomaly 58

Characteristics:

Orphanet epidemiological data:

58

Classifications:

Orphanet: 58  
Rare endocrine diseases


External Ids:

ICD10 via Orphanet 33 E03.1
Orphanet 58 ORPHA95711

Summaries for Congenital Hypothyroidism Due to Developmental Anomaly

MalaCards based summary : Congenital Hypothyroidism Due to Developmental Anomaly, is also known as primary congenital hypothyroidism due to developmental anomaly. Affiliated tissues include thyroid.

Symptoms & Phenotypes for Congenital Hypothyroidism Due to Developmental Anomaly

Drugs & Therapeutics for Congenital Hypothyroidism Due to Developmental Anomaly

Search Clinical Trials , NIH Clinical Center for Congenital Hypothyroidism Due to Developmental Anomaly

Genetic Tests for Congenital Hypothyroidism Due to Developmental Anomaly

Anatomical Context for Congenital Hypothyroidism Due to Developmental Anomaly

MalaCards organs/tissues related to Congenital Hypothyroidism Due to Developmental Anomaly:

40
Thyroid

Publications for Congenital Hypothyroidism Due to Developmental Anomaly

Variations for Congenital Hypothyroidism Due to Developmental Anomaly

Expression for Congenital Hypothyroidism Due to Developmental Anomaly

Search GEO for disease gene expression data for Congenital Hypothyroidism Due to Developmental Anomaly.

Pathways for Congenital Hypothyroidism Due to Developmental Anomaly

GO Terms for Congenital Hypothyroidism Due to Developmental Anomaly

Sources for Congenital Hypothyroidism Due to Developmental Anomaly

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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