MYMY3
MCID: MYM005
MIFTS: 11

Moyamoya Disease 3 (MYMY3)

Categories: Cardiovascular diseases, Genetic diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Moyamoya Disease 3

MalaCards integrated aliases for Moyamoya Disease 3:

Name: Moyamoya Disease 3 58 13 74
Mymy3 58

Classifications:



External Ids:

OMIM 58 608796
UMLS 74 C1837418

Summaries for Moyamoya Disease 3

OMIM : 58 In moyamoya disease, stenosis of the intracranial portion of the internal carotid artery leads to secondary establishment of intracranial compensatory anastomoses at different levels (leptomeninges, basal ganglia, and transdural) (summary by Sakurai et al., 2004). For a general phenotypic description and a discussion of genetic heterogeneity of moyamoya disease, see MYMY1 (252350). (608796)

MalaCards based summary : Moyamoya Disease 3, also known as mymy3, is related to moyamoya disease 1 and cone-rod dystrophy and hearing loss 2. An important gene associated with Moyamoya Disease 3 is MYMY3 (Moyamoya Disease 3).

Related Diseases for Moyamoya Disease 3

Diseases in the Moyamoya Disease 1 family:

Moyamoya Disease 2 Moyamoya Disease 3
Moyamoya Disease 5

Diseases related to Moyamoya Disease 3 via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 moyamoya disease 1 11.1
2 cone-rod dystrophy and hearing loss 2 11.1

Symptoms & Phenotypes for Moyamoya Disease 3

Clinical features from OMIM:

608796

Drugs & Therapeutics for Moyamoya Disease 3

Search Clinical Trials , NIH Clinical Center for Moyamoya Disease 3

Genetic Tests for Moyamoya Disease 3

Anatomical Context for Moyamoya Disease 3

Publications for Moyamoya Disease 3

Variations for Moyamoya Disease 3

Expression for Moyamoya Disease 3

Search GEO for disease gene expression data for Moyamoya Disease 3.

Pathways for Moyamoya Disease 3

GO Terms for Moyamoya Disease 3

Sources for Moyamoya Disease 3

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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