MCID: HRD205
MIFTS: 6

Hereditary Lymphedema Ib

Categories: Cardiovascular diseases, Fetal diseases, Genetic diseases, Immune diseases, Rare diseases, Skin diseases

Aliases & Classifications for Hereditary Lymphedema Ib

MalaCards integrated aliases for Hereditary Lymphedema Ib:

Name: Hereditary Lymphedema Ib 12
Lmph1b 12

Classifications:



External Ids:

Disease Ontology 12 DOID:0070211

Summaries for Hereditary Lymphedema Ib

Disease Ontology : 12 A hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in the chromosomal region 6q16.2-q22.1.

MalaCards based summary : Hereditary Lymphedema Ib, also known as lmph1b, is related to lymphatic malformation 2.

Related Diseases for Hereditary Lymphedema Ib

Diseases in the Primary Lymphedema family:

Hereditary Lymphedema Hereditary Lymphedema Ic
Hereditary Lymphedema Id Hereditary Lymphedema Ia
Hereditary Lymphedema Ib Hereditary Lymphedema I
Hereditary Lymphedema Ii Congenital Lymphedema
Celsr1-Related Late-Onset Primary Lymphedema Gjc2-Related Late-Onset Primary Lymphedema

Diseases related to Hereditary Lymphedema Ib via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 lymphatic malformation 2 11.4

Symptoms & Phenotypes for Hereditary Lymphedema Ib

Drugs & Therapeutics for Hereditary Lymphedema Ib

Search Clinical Trials , NIH Clinical Center for Hereditary Lymphedema Ib

Genetic Tests for Hereditary Lymphedema Ib

Anatomical Context for Hereditary Lymphedema Ib

Publications for Hereditary Lymphedema Ib

Variations for Hereditary Lymphedema Ib

Expression for Hereditary Lymphedema Ib

Search GEO for disease gene expression data for Hereditary Lymphedema Ib.

Pathways for Hereditary Lymphedema Ib

GO Terms for Hereditary Lymphedema Ib

Sources for Hereditary Lymphedema Ib

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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