MCID: OVR071
MIFTS: 4

Ovarian Insufficiency, Familial

Categories: Endocrine diseases, Genetic diseases, Rare diseases, Reproductive diseases

Aliases & Classifications for Ovarian Insufficiency, Familial

MalaCards integrated aliases for Ovarian Insufficiency, Familial:

Name: Ovarian Insufficiency, Familial 20

Classifications:



Summaries for Ovarian Insufficiency, Familial

MalaCards based summary : Ovarian Insufficiency, Familial Affiliated tissues include Ovary.

Symptoms & Phenotypes for Ovarian Insufficiency, Familial

Drugs & Therapeutics for Ovarian Insufficiency, Familial

Search Clinical Trials , NIH Clinical Center for Ovarian Insufficiency, Familial

Genetic Tests for Ovarian Insufficiency, Familial

Anatomical Context for Ovarian Insufficiency, Familial

MalaCards organs/tissues related to Ovarian Insufficiency, Familial:

40
Ovary
LifeMap Discovery
Data from LifeMap, the Embryonic Development and Stem Cells Database

Cells/anatomical compartments in embryo or adult related to Ovarian Insufficiency, Familial:
# Tissue Anatomical CompartmentCell Relevance
1 Ovary Secondary Follicle Affected by disease

Publications for Ovarian Insufficiency, Familial

Variations for Ovarian Insufficiency, Familial

Expression for Ovarian Insufficiency, Familial

Search GEO for disease gene expression data for Ovarian Insufficiency, Familial.

Pathways for Ovarian Insufficiency, Familial

GO Terms for Ovarian Insufficiency, Familial

Sources for Ovarian Insufficiency, Familial

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
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
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 20-May-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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