MCID: LNG103
MIFTS: 6

Lin-Gettig Syndrome

Categories: Rare diseases

Aliases & Classifications for Lin-Gettig Syndrome

MalaCards integrated aliases for Lin-Gettig Syndrome:

Name: Lin-Gettig Syndrome 53
Craniosynostosis-Intellectual Disability Syndrome of Lin and Gettig 53

Classifications:



Summaries for Lin-Gettig Syndrome

MalaCards based summary : Lin-Gettig Syndrome, also known as craniosynostosis-intellectual disability syndrome of lin and gettig, is related to craniosynostosis. An important gene associated with Lin-Gettig Syndrome is KAT6B (Lysine Acetyltransferase 6B).

Related Diseases for Lin-Gettig Syndrome

Diseases related to Lin-Gettig Syndrome via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 craniosynostosis 10.2

Symptoms & Phenotypes for Lin-Gettig Syndrome

Drugs & Therapeutics for Lin-Gettig Syndrome

Search Clinical Trials , NIH Clinical Center for Lin-Gettig Syndrome

Genetic Tests for Lin-Gettig Syndrome

Anatomical Context for Lin-Gettig Syndrome

Publications for Lin-Gettig Syndrome

Articles related to Lin-Gettig Syndrome:

# Title Authors Year
1
Lin-Gettig syndrome: Craniosynostosis expands the spectrum of the KAT6B related disorders. ( 28696035 )
2017
2
Possible third case of Lin-Gettig syndrome. ( 12116213 )
2002

Variations for Lin-Gettig Syndrome

Expression for Lin-Gettig Syndrome

Search GEO for disease gene expression data for Lin-Gettig Syndrome.

Pathways for Lin-Gettig Syndrome

GO Terms for Lin-Gettig Syndrome

Sources for Lin-Gettig 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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