MCID: CRB052
MIFTS: 8

Carbon Baby Syndrome

Categories: Rare diseases

Aliases & Classifications for Carbon Baby Syndrome

MalaCards integrated aliases for Carbon Baby Syndrome:

Name: Carbon Baby Syndrome 53
Universal Acquired Melanosis 53 73

Classifications:



External Ids:

UMLS 73 C0406419

Summaries for Carbon Baby Syndrome

NIH Rare Diseases : 53 Carbon baby syndrome, also known as universal acquired melanosis, is a rare form of hyperpigmentation. The skin of affected infants progressively darkens over the first years of life in the absence of other symptoms. The cause of the condition is unknown. 

MalaCards based summary : Carbon Baby Syndrome, is also known as universal acquired melanosis. Affiliated tissues include skin.

Related Diseases for Carbon Baby Syndrome

Symptoms & Phenotypes for Carbon Baby Syndrome

Drugs & Therapeutics for Carbon Baby Syndrome

Search Clinical Trials , NIH Clinical Center for Carbon Baby Syndrome

Genetic Tests for Carbon Baby Syndrome

Anatomical Context for Carbon Baby Syndrome

MalaCards organs/tissues related to Carbon Baby Syndrome:

41
Skin

Publications for Carbon Baby Syndrome

Articles related to Carbon Baby Syndrome:

# Title Authors Year
1
Acquired Universal Melanosis (Carbon Baby Syndrome). ( 23331086 )
2013
2
Universal acquired melanosis: carbon baby. ( 24010507 )
2013
3
Universal acquired melanosis in siblings. ( 21975657 )
2012
4
Carbon baby syndrome (universal acquired melanosis). ( 22253152 )
2011
5
Universal acquired melanosis (Carbon baby). ( 18187822 )
2008
6
Universal acquired melanosis. The carbon baby. ( 646402 )
1978

Variations for Carbon Baby Syndrome

Expression for Carbon Baby Syndrome

Search GEO for disease gene expression data for Carbon Baby Syndrome.

Pathways for Carbon Baby Syndrome

GO Terms for Carbon Baby Syndrome

Sources for Carbon Baby Syndrome

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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