MCID: ALD006
MIFTS: 6

Aldred Syndrome

Categories: Mental diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Aldred Syndrome

MalaCards integrated aliases for Aldred Syndrome:

Name: Aldred Syndrome 52 71
Retinitis Pigmentosa and Intellectual Disability Due to Xp11.3 Microdeletion 52
X-Linked Intellectual Disability-Retinitis Pigmentosa Syndrome 52
Retinitis Pigmentosa and Intellectual Disability Due to Del 52
X-Linked Mental Handicap-Retinitis Pigmentosa Syndrome 52

Classifications:



External Ids:

UMLS 71 C0795873

Summaries for Aldred Syndrome

MalaCards based summary : Aldred Syndrome, also known as retinitis pigmentosa and intellectual disability due to xp11.3 microdeletion, is related to chromosome xp11.3 deletion syndrome.

Wikipedia : 74 Aldred syndrome is an X-linked recessive genetic disorder. It is mainly characterized by a form of... more...

Related Diseases for Aldred Syndrome

Diseases related to Aldred Syndrome via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 chromosome xp11.3 deletion syndrome 11.4

Symptoms & Phenotypes for Aldred Syndrome

Drugs & Therapeutics for Aldred Syndrome

Search Clinical Trials , NIH Clinical Center for Aldred Syndrome

Genetic Tests for Aldred Syndrome

Anatomical Context for Aldred Syndrome

Publications for Aldred Syndrome

Variations for Aldred Syndrome

Expression for Aldred Syndrome

Search GEO for disease gene expression data for Aldred Syndrome.

Pathways for Aldred Syndrome

GO Terms for Aldred Syndrome

Sources for Aldred Syndrome

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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