MCID: HLL012
MIFTS: 10

Hallermann-Streiff-Like Syndrome

Categories: Bone diseases, Eye diseases, Fetal diseases, Genetic diseases, Neuronal diseases, Rare diseases, Skin diseases

Aliases & Classifications for Hallermann-Streiff-Like Syndrome

MalaCards integrated aliases for Hallermann-Streiff-Like Syndrome:

Name: Hallermann-Streiff-Like Syndrome 58
Dennis-Fairhurst-Moore Syndrome 58 29
Hallermann-Streiff-Francois Syndrome, Severe Form 58
Severe Hallermann-Streiff-Francois Syndrome 58
Dennis Fairhurst Moore Syndrome 71

Classifications:

Orphanet: 58  
Rare neurological diseases
Rare eye diseases
Rare bone diseases
Rare skin diseases
Developmental anomalies during embryogenesis


External Ids:

ICD10 via Orphanet 33 Q87.0
UMLS via Orphanet 72 C2931775
Orphanet 58 ORPHA2109
UMLS 71 C2931775

Summaries for Hallermann-Streiff-Like Syndrome

MalaCards based summary : Hallermann-Streiff-Like Syndrome, is also known as dennis-fairhurst-moore syndrome. Affiliated tissues include eye, bone and skin.

Related Diseases for Hallermann-Streiff-Like Syndrome

Diseases in the Hallermann-Streiff Syndrome family:

Hallermann-Streiff-Like Syndrome

Symptoms & Phenotypes for Hallermann-Streiff-Like Syndrome

Drugs & Therapeutics for Hallermann-Streiff-Like Syndrome

Search Clinical Trials , NIH Clinical Center for Hallermann-Streiff-Like Syndrome

Genetic Tests for Hallermann-Streiff-Like Syndrome

Genetic tests related to Hallermann-Streiff-Like Syndrome:

# Genetic test Affiliating Genes
1 Dennis-Fairhurst-Moore Syndrome 29

Anatomical Context for Hallermann-Streiff-Like Syndrome

MalaCards organs/tissues related to Hallermann-Streiff-Like Syndrome:

40
Eye, Bone, Skin

Publications for Hallermann-Streiff-Like Syndrome

Variations for Hallermann-Streiff-Like Syndrome

Expression for Hallermann-Streiff-Like Syndrome

Search GEO for disease gene expression data for Hallermann-Streiff-Like Syndrome.

Pathways for Hallermann-Streiff-Like Syndrome

GO Terms for Hallermann-Streiff-Like Syndrome

Sources for Hallermann-Streiff-Like 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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