MCID: OBS190
MIFTS: 4

Obsolete: Retinitis Pigmentosa and Intellectual Disability Due to Monosomy Xp11.3

Categories: Rare diseases

Aliases & Classifications for Obsolete: Retinitis Pigmentosa and Intellectual Disability Due to...

MalaCards integrated aliases for Obsolete: Retinitis Pigmentosa and Intellectual Disability Due to Monosomy Xp11.3:

Name: Obsolete: Retinitis Pigmentosa and Intellectual Disability Due to Monosomy Xp11.3 58
Retinitis Pigmentosa and Intellectual Disability Due to Xp11.3 Microdeletion 58
Retinitis Pigmentosa and Intellectual Disability Due to Del 58

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External Ids:

Orphanet 58 ORPHA261512

Summaries for Obsolete: Retinitis Pigmentosa and Intellectual Disability Due to...

MalaCards based summary : Obsolete: Retinitis Pigmentosa and Intellectual Disability Due to Monosomy Xp11.3, also known as retinitis pigmentosa and intellectual disability due to xp11.3 microdeletion, is related to chromosome xp11.3 deletion syndrome and aldred syndrome.

Related Diseases for Obsolete: Retinitis Pigmentosa and Intellectual Disability Due to...

Diseases related to Obsolete: Retinitis Pigmentosa and Intellectual Disability Due to Monosomy Xp11.3 via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 chromosome xp11.3 deletion syndrome 11.7
2 aldred syndrome 11.7

Symptoms & Phenotypes for Obsolete: Retinitis Pigmentosa and Intellectual Disability Due to...

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Search Clinical Trials , NIH Clinical Center for Obsolete: Retinitis Pigmentosa and Intellectual Disability Due to Monosomy Xp11.3

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Expression for Obsolete: Retinitis Pigmentosa and Intellectual Disability Due to...

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GO Terms for Obsolete: Retinitis Pigmentosa and Intellectual Disability Due to...

Sources for Obsolete: Retinitis Pigmentosa and Intellectual Disability Due to...

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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