MCID: OVR071
MIFTS: 5

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 52

Classifications:



Summaries for Ovarian Insufficiency, Familial

MalaCards based summary : Ovarian Insufficiency, Familial is related to premature ovarian failure 1 and azoospermia. An important gene associated with Ovarian Insufficiency, Familial is FMR1 (FMRP Translational Regulator 1). Affiliated tissues include Ovary.

Related Diseases for Ovarian Insufficiency, Familial

Diseases in the Ovarian Disease family:

Ovarian Insufficiency, Familial

Diseases related to Ovarian Insufficiency, Familial via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 premature ovarian failure 1 11.7
2 azoospermia 9.8

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

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
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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