MCID: SCH034
MIFTS: 6

Schwartz Cohen-Addad Lambert Syndrome

Categories: Rare diseases

Aliases & Classifications for Schwartz Cohen-Addad Lambert Syndrome

MalaCards integrated aliases for Schwartz Cohen-Addad Lambert Syndrome:

Name: Schwartz Cohen-Addad Lambert Syndrome 52 71
Congenital Melanocytosis with Myelomeningocele and Hydrocephalus 52

Classifications:



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UMLS 71 C2931036

Summaries for Schwartz Cohen-Addad Lambert Syndrome

MalaCards based summary : Schwartz Cohen-Addad Lambert Syndrome, also known as congenital melanocytosis with myelomeningocele and hydrocephalus, is related to dowling-degos disease 1 and myelomeningocele.

Related Diseases for Schwartz Cohen-Addad Lambert Syndrome

Diseases related to Schwartz Cohen-Addad Lambert Syndrome via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 dowling-degos disease 1 10.2
2 myelomeningocele 10.2
3 hydrocephalus 10.2
4 mongolian spot 10.2

Symptoms & Phenotypes for Schwartz Cohen-Addad Lambert Syndrome

Drugs & Therapeutics for Schwartz Cohen-Addad Lambert Syndrome

Search Clinical Trials , NIH Clinical Center for Schwartz Cohen-Addad Lambert Syndrome

Genetic Tests for Schwartz Cohen-Addad Lambert Syndrome

Anatomical Context for Schwartz Cohen-Addad Lambert Syndrome

Publications for Schwartz Cohen-Addad Lambert Syndrome

Articles related to Schwartz Cohen-Addad Lambert Syndrome:

# Title Authors PMID Year
1
Congenital melanocytosis with myelomeningocele and hydrocephalus. 61
3948532 1986

Variations for Schwartz Cohen-Addad Lambert Syndrome

Expression for Schwartz Cohen-Addad Lambert Syndrome

Search GEO for disease gene expression data for Schwartz Cohen-Addad Lambert Syndrome.

Pathways for Schwartz Cohen-Addad Lambert Syndrome

GO Terms for Schwartz Cohen-Addad Lambert Syndrome

Sources for Schwartz Cohen-Addad Lambert 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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