MCID: PRM001
MIFTS: 44

Primary Cutaneous Amyloidosis

Categories: Rare diseases, Skin diseases, Metabolic diseases, Genetic diseases

Aliases & Classifications for Primary Cutaneous Amyloidosis

MalaCards integrated aliases for Primary Cutaneous Amyloidosis:

Name: Primary Cutaneous Amyloidosis 12 50 25 14
Familial Primary Localized Cutaneous Amyloidosis 12 56
Primary Localized Cutaneous Amyloidosis 50 25
Amyloidosis, Primary Cutaneous 52 69
Amyloidosis Ix 50 25
Plca 50 25
Amyloidosis Familial Cutaneous Lichen 50
Lichen Amyloidosis Familial 50
Familial Lichen Amyloidosis 69
Amyloidosis 9 50
Fplca 56
Pca 12

Characteristics:

Orphanet epidemiological data:

56
familial primary localized cutaneous amyloidosis
Inheritance: Autosomal dominant; Age of onset: All ages;

Classifications:

Orphanet: 56  
Rare skin diseases


External Ids:

Disease Ontology 12 DOID:0050639
Orphanet 56 ORPHA353220
ICD10 via Orphanet 34 E85.4+ L99.0*

Summaries for Primary Cutaneous Amyloidosis

NIH Rare Diseases : 50 primary cutaneous amyloidosis is a form of amyloidosis, a group of conditions in which an abnormal protein (called amyloid) builds up in various organs and tissues throughout the body. in primary cutaneous amyloidosis, specifically, this protein accumulates in the skin. there are three main forms of primary cutaneous amyloidosis:lichen amyloidosis - multiple itchy, raised spots which are scaly and red/brown in color. this rash generally affects the shins, thighs, feet and forearms. macular amyloidosis - mild to severely itchy, flat, dusky-brown or greyish colored spots that may come together to form patches of darkened skin. this rash generally appears on the upper back between the shoulder blades, the chest and less commonly, the arms. nodular amyloidosis - asymptomatic firm bumps that may be pinkish-brown to red in color. this rash may occur on the trunk, limbs, face, and/or genitals. the exact underlying cause of primary cutaneous amyloidosis is poorly understood. it is sometimes associated with other conditions such as atopic dermatitis, sarcoidosis, and psoriasis. although most cases occur sporadically in people with no family history of the condition, there are rare familial forms caused by changes (mutations) in the osmr or il31ra gene. treatment is based on the signs and symptoms present in each person and may include surgery to remove amyloid deposits and/or certain medications to relieve itching. last updated: 3/29/2016

MalaCards based summary : Primary Cutaneous Amyloidosis, also known as familial primary localized cutaneous amyloidosis, is related to posterior cortical atrophy and amyloidosis, primary localized cutaneous, 1. An important gene associated with Primary Cutaneous Amyloidosis is OSMR (Oncostatin M Receptor), and among its related pathways/superpathways are Cytokine Signaling in Immune system and Developmental Biology. The drugs Methylene blue and Pharmaceutical Solutions have been mentioned in the context of this disorder. Affiliated tissues include skin and b cells, and related phenotypes are Decreased shRNA abundance (Z-score < -2) and digestive/alimentary

Genetics Home Reference : 25 Primary localized cutaneous amyloidosis (PLCA) is a condition in which clumps of abnormal proteins called amyloids build up in the skin, specifically in the wave-like projections (dermal papillae) between the top two layers of skin (the dermis and the epidermis). The primary feature of PLCA is patches of skin with abnormal texture or color. The appearance of these patches defines three forms of the condition: lichen amyloidosis, macular amyloidosis, and nodular amyloidosis.

Disease Ontology : 12 An amyloidosis characterized by pruritus, skin scratching and by deposits of amyloid in the dermis.

Wikipedia : 72 Primary cutaneous amyloidosis is a form of amyloidosis associated with oncostatin M receptor. This type... more...

Related Diseases for Primary Cutaneous Amyloidosis

Diseases in the Primary Cutaneous Amyloidosis family:

Amyloidosis, Primary Localized Cutaneous, 1 Amyloidosis, Primary Localized Cutaneous, 2

Diseases related to Primary Cutaneous Amyloidosis via text searches within MalaCards or GeneCards Suite gene sharing:

(show top 50) (show all 128)
id Related Disease Score Top Affiliating Genes
1 posterior cortical atrophy 11.7
2 amyloidosis, primary localized cutaneous, 1 11.0
3 autism-facial port-wine stain syndrome 11.0 IL31RA OSMR
4 ercc2-related xeroderma pigmentosum 10.9 KRT14 KRT5
5 pachyonychia congenita 3 10.8 KRT14 KRT5
6 cervical spina bifida cystica 10.8 KRT18 KRT8
7 serotonin syndrome 10.8 IL31 IL31RA OSMR
8 fallopian tube transitional cell carcinoma 10.8 KRT18 KRT5
9 dowling-degos disease 1 10.8 KRT14 KRT5
10 hypotrichosis 13 10.8 KRT18 KRT8
11 infiltrative basal cell carcinoma 10.8 KRT17 KRT7
12 adult mesoblastic nephroma 10.8 KRT17 KRT18
13 chronic rapidly progressive glomerulonephritis 10.8 KRT19 KRT8
14 cervical adenitis 10.8 KRT5 KRT7
15 steatocystoma multiplex 10.8 KRT16 KRT17
16 dicrocoeliasis 10.8 KRT16 KRT17
17 endometrial disease 10.8 KRT5 KRT7
18 engraftment syndrome 10.7 KRT7 KRT8
19 lipid-cell variant infiltrating bladder urothelial carcinoma 10.7 KRT5 KRT7
20 basal cell carcinoma 4 10.7 KRT16 KRT17
21 cribriform carcinoma 10.7 KRT18 KRT5 KRT8
22 light chain deposition disease 10.7 KRT14 KRT5
23 small intestine leiomyoma 10.7 KRT17 KRT5
24 eccrine acrospiroma 10.7 KRT19 KRT7
25 congenital hemolytic anemia 10.7 KRT14 KRT5 KRT8
26 breast cystic hypersecretory carcinoma 10.7 KRT19 KRT7
27 sebaceous adenocarcinoma 10.7 KRT18 KRT5 KRT8
28 familial periodic paralysis 10.6 KRT5 KRT7 KRT8
29 sclerosteosis 1 10.6 KRT10 KRT16 KRT17
30 anal paget's disease 10.6 KRT14 KRT18 KRT8
31 boylan dew greco syndrome 10.6 KRT10 KRT16 KRT17
32 mucoepidermoid esophageal carcinoma 10.6 KRT5 KRT7
33 childhood type dermatomyositis 10.6 KRT17 KRT8 OSMR
34 cervix erosion 10.6 KRT19 KRT7
35 penis squamous cell carcinoma 10.6 KRT10 KRT14 KRT5
36 urinary bladder inverted papilloma 10.6 KRT14 KRT19
37 vulva adenocarcinoma 10.6 KRT14 KRT5 KRT8
38 anaerobic pneumonia 10.6 KRT14 KRT17 KRT5
39 middle ear squamous cell carcinoma 10.6 KRT14 KRT17 KRT8
40 kidney clear cell sarcoma 10.6 KRT5 KRT7 KRT8
41 epidermolysis bullosa simplex, koebner type 10.6 KRT10 KRT14 KRT5
42 superior mesenteric artery syndrome 10.6 KRT5 KRT7 KRT8
43 pigmented basal cell carcinoma 10.6 KRT10 KRT14 KRT17
44 female breast axillary tail cancer 10.6 KRT14 KRT5 KRT7
45 colon squamous cell carcinoma 10.6 KRT5 KRT7 KRT8
46 lobular neoplasia 10.6 KRT14 KRT5 KRT7
47 klatskin's tumor 10.6 KRT5 KRT7 KRT8
48 palmoplantar keratoderma, nonepidermolytic, focal 10.6 KRT10 KRT16 KRT17
49 lacrimal gland mucoepidermoid carcinoma 10.6 KRT10 KRT14 KRT5
50 epidermolysis bullosa simplex-mp 10.6 KRT14 KRT5

Graphical network of the top 20 diseases related to Primary Cutaneous Amyloidosis:



Diseases related to Primary Cutaneous Amyloidosis

Symptoms & Phenotypes for Primary Cutaneous Amyloidosis

GenomeRNAi Phenotypes related to Primary Cutaneous Amyloidosis according to GeneCards Suite gene sharing:

26
id Description GenomeRNAi Source Accession Score Top Affiliating Genes
1 Decreased shRNA abundance (Z-score < -2) GR00366-A-153 9.58 KRT5
2 Decreased shRNA abundance (Z-score < -2) GR00366-A-154 9.58 KRT18
3 Decreased shRNA abundance (Z-score < -2) GR00366-A-17 9.58 KRT18 KRT5
4 Decreased shRNA abundance (Z-score < -2) GR00366-A-180 9.58 KRT5 KRT8
5 Decreased shRNA abundance (Z-score < -2) GR00366-A-200 9.58 KRT5
6 Decreased shRNA abundance (Z-score < -2) GR00366-A-33 9.58 KRT18
7 Decreased shRNA abundance (Z-score < -2) GR00366-A-40 9.58 KRT8
8 Decreased shRNA abundance (Z-score < -2) GR00366-A-68 9.58 KRT7
9 Decreased shRNA abundance (Z-score < -2) GR00366-A-71 9.58 KRT18 KRT5 KRT7 KRT8
10 Decreased shRNA abundance (Z-score < -2) GR00366-A-72 9.58 KRT7
11 Decreased shRNA abundance (Z-score < -2) GR00366-A-84 9.58 KRT18
12 Decreased shRNA abundance (Z-score < -2) GR00366-A-91 9.58 KRT5 KRT7

MGI Mouse Phenotypes related to Primary Cutaneous Amyloidosis:

44
id Description MGI Source Accession Score Top Affiliating Genes
1 digestive/alimentary MP:0005381 9.17 KRT14 KRT16 KRT17 KRT19 KRT5 KRT8

Drugs & Therapeutics for Primary Cutaneous Amyloidosis

Drugs for Primary Cutaneous Amyloidosis (from DrugBank, HMDB, Dgidb, PharmGKB, IUPHAR, NovoSeek, BitterDB):


id Name Status Phase Clinical Trials Cas Number PubChem Id
1
Methylene blue Investigational 61-73-4
2 Pharmaceutical Solutions

Interventional clinical trials:


id Name Status NCT ID Phase Drugs
1 Efficacy of 308-nm Excimer Laser for Primary Localized Cutaneous Amyloidosis Treatment in Asians Recruiting NCT03068156
2 Efficacy of Methylene Blue Mediated Photodynamic Therapy for Primary Localized Cutaneous Amyloidosis Treatment in Asians Not yet recruiting NCT03068208

Search NIH Clinical Center for Primary Cutaneous Amyloidosis

Genetic Tests for Primary Cutaneous Amyloidosis

Anatomical Context for Primary Cutaneous Amyloidosis

MalaCards organs/tissues related to Primary Cutaneous Amyloidosis:

39
Skin, B Cells

Publications for Primary Cutaneous Amyloidosis

Articles related to Primary Cutaneous Amyloidosis:

(show top 50) (show all 60)
id Title Authors Year
1
Reflectance confocal microscopy for the characterization of primary cutaneous amyloidosis: a pilot study. ( 28083882 )
2017
2
Comparative proteomics analysis of primary cutaneous amyloidosis. ( 28912854 )
2017
3
Treatment of primary cutaneous amyloidosis with laser: a review of the literature. ( 26984345 )
2016
4
Health-related quality of life in patients with primary cutaneous amyloidosis. ( 25799390 )
2015
5
Efficacy of different modes of fractional CO2 laser in the treatment of primary cutaneous amyloidosis: A randomized clinical trial. ( 25946210 )
2015
6
Unilateral primary cutaneous amyloidosis of the eyelid masquerading as a chalazion. ( 25284111 )
2014
7
Nodular localized primary cutaneous amyloidosis: a bullous variant. ( 24635076 )
2014
8
Amyloidosis cutis dyschromia: a rare form of primary cutaneous amyloidosis. ( 24746296 )
2014
9
Reactive eccrine syringofibroadenomatosis secondary to primary cutaneous amyloidosis: a novel association. ( 24325801 )
2013
10
Primary cutaneous amyloidosis of the glans penis. Two case reports and a review of the literature. ( 24125073 )
2013
11
MCP-1 as an effector of IL-31 signaling in familial primary cutaneous amyloidosis. ( 23303452 )
2013
12
Thalidomide improves clinical symptoms of primary cutaneous amyloidosis: report of familiar and sporadic cases. ( 23742287 )
2013
13
Primary cutaneous amyloidosis of the external ear: a clinicopathological and immunohistochemical study of 17 cases. ( 22077601 )
2012
14
Poikiloderma-like primary cutaneous amyloidosis confined to the calves in a Chinese man. ( 22776500 )
2012
15
Primary cutaneous amyloidosis: a clinico-pathological study with emphasis on polarized microscopy. ( 22771637 )
2012
16
Characteristic dermoscopic features of primary cutaneous amyloidosis: a study of 35 cases. ( 22632408 )
2012
17
Role of oligomers in the amyloidogenesis of primary cutaneous amyloidosis. ( 21669474 )
2011
18
Nodular localized primary cutaneous amyloidosis and primary marginal zone B-cell lymphoma on the nose: treatment with microscopically controlled surgery. ( 21413960 )
2011
19
Association of primary cutaneous amyloidosis with atopic dermatitis: a nationwide population-based study in Taiwan. ( 21070198 )
2011
20
Dramatic improvement of primary cutaneous amyloidosis with thalidomide. ( 21382777 )
2011
21
Unusual primary cutaneous amyloidosis with an incontinentia pigmenti-like pattern. ( 21413964 )
2011
22
A rare type of primary cutaneous amyloidosis: amyloidosis cutis dyschromica. ( 21091677 )
2010
23
Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis. ( 19690585 )
2010
24
Identification of an oncostatin M receptor mutation associated with familial primary cutaneous amyloidosis. ( 19466957 )
2009
25
Papules and plaques on the nose. Nodular localized primary cutaneous amyloidosis. ( 17438189 )
2007
26
A comparative study of two Congo red stains for the detection of primary cutaneous amyloidosis. ( 16844537 )
2006
27
Primary cutaneous amyloidosis of the auricular concha: case report and review of published work. ( 16556282 )
2006
28
Genome-wide scan identifies a susceptibility locus for familial primary cutaneous amyloidosis on chromosome 5p13.1-q11.2. ( 17107390 )
2006
29
Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23. ( 15656797 )
2005
30
Primary cutaneous amyloidosis. ( 11991040 )
2002
31
Nodular localized primary cutaneous amyloidosis. ( 12174132 )
2002
32
Nodular localized primary cutaneous amyloidosis: a long-term follow-up study. ( 11453916 )
2001
33
Clinical and histopathological characteristics of primary cutaneous amyloidosis in 794 Chinese patients. ( 11355326 )
2001
34
Primary cutaneous amyloidosis involving the external ears along with the classical sites. ( 17664705 )
2001
35
Apoptosis in primary cutaneous amyloidosis. ( 10733268 )
1999
36
Familial primary cutaneous amyloidosis in a South African family. ( 10606942 )
1999
37
Cytokeratins in primary cutaneous amyloidosis. ( 9611375 )
1998
38
Primary cutaneous amyloidosis. ( 20944287 )
1997
39
Detection of Epstein-Barr virus in primary cutaneous amyloidosis. ( 9217811 )
1997
40
Epstein-Barr virus-related primary cutaneous amyloidosis. Successful treatment with acyclovir and interferon-alpha. ( 8745909 )
1996
41
Genetic heterogeneity of familial primary cutaneous amyloidosis: lack of evidence for linkage with the chromosome 10 pericentromeric region in Chinese families. ( 8752835 )
1996
42
Unusual manifestations of primary cutaneous amyloidosis in association with Raynaud's phenomenon and livedo reticularis. ( 1516235 )
1992
43
Diffuse primary cutaneous amyloidosis. ( 1476924 )
1992
44
Partial amino acid sequence of an amyloid fibril protein from nodular primary cutaneous amyloidosis showing homology to lambda immunoglobulin light chain of variable subgroup III (a lambda III). ( 2117035 )
1990
45
Primary cutaneous amyloidosis of the auricular concha. ( 3279082 )
1988
46
A monoclonal anti-keratin antibody reactive with amyloid deposit of primary cutaneous amyloidosis. ( 2449480 )
1987
47
Nodular localized primary cutaneous amyloidosis. ( 3504756 )
1987
48
Primary cutaneous amyloidosis. ( 3553043 )
1987
49
Nodular primary cutaneous amyloidosis. Isolation and characterization of amyloid fibrils. ( 3789778 )
1986
50
Primary cutaneous amyloidosis: identically distributed lesions in identical twins. ( 3725702 )
1986

Variations for Primary Cutaneous Amyloidosis

Expression for Primary Cutaneous Amyloidosis

Search GEO for disease gene expression data for Primary Cutaneous Amyloidosis.

Pathways for Primary Cutaneous Amyloidosis

Pathways related to Primary Cutaneous Amyloidosis according to GeneCards Suite gene sharing:

(show all 46)
id Super pathways Score Top Affiliating Genes
1
Show member pathways
13.33 CALM1 CALM2 CALM3 CCL2 IL31 IL31RA
2
Show member pathways
13.15 CALM1 CALM2 CALM3 KRT10 KRT14 KRT16
3
Show member pathways
12.81 CALM1 CALM2 CALM3 MYLK TNNT1
4
Show member pathways
12.4 CALM1 CALM2 CALM3 MYLK
5
Show member pathways
12.37 CALM1 CALM2 CALM3 MYLK
6
Show member pathways
12.29 CALM1 CALM2 CALM3 MYLK
7 12.28 KRT10 KRT17 KRT18 KRT19 KRT5 KRT7
8
Show member pathways
12.19 CALM1 CALM2 CALM3 MYLK
9
Show member pathways
12.12 CALM1 CALM2 CALM3 MYLK
10
Show member pathways
12.06 KRT10 KRT14 KRT16 KRT17 KRT18 KRT19
11 12.04 CALM1 CALM2 CALM3 CCL2
12 12.02 CALM1 CALM2 CALM3 MYLK
13
Show member pathways
11.9 CALM1 CALM2 CALM3
14 11.88 CALM1 CALM2 CALM3
15 11.88 CALM1 CALM2 CALM3
16
Show member pathways
11.85 CALM1 CALM2 CALM3
17
Show member pathways
11.82 CALM1 CALM2 CALM3
18
Show member pathways
11.81 CALM1 CALM2 CALM3
19
Show member pathways
11.78 CALM1 CALM2 CALM3
20 11.76 KRT14 KRT17 KRT5
21
Show member pathways
11.74 CALM1 CALM2 CALM3
22
Show member pathways
11.73 CALM1 CALM2 CALM3
23
Show member pathways
11.72 CALM1 CALM2 CALM3
24 11.71 CALM1 CALM2 CALM3
25
Show member pathways
11.7 CALM1 CALM2 CALM3
26 11.69 CALM1 CALM2 CALM3
27
Show member pathways
11.64 CALM1 CALM2 CALM3
28 11.62 CALM1 CALM2 CALM3
29 11.6 CALM1 CALM2 CALM3
30
Show member pathways
11.58 CALM1 CALM2 CALM3
31 11.5 CALM1 CALM2 CALM3 MYLK
32 11.49 CALM1 CALM2 CALM3
33 11.3 CALM1 CALM2 CALM3
34 11.28 CALM1 CALM2 CALM3
35 11.26 CALM1 CALM2 MYLK
36
Show member pathways
11.26 KRT14 KRT16 KRT17 KRT18 KRT19 KRT5
37 11.23 CALM1 CALM2 CALM3
38 11.19 CALM1 CALM2 CALM3
39 11.18 CALM1 CALM2 CALM3 MYLK
40 11.15 CALM1 CALM2 CALM3
41 11.13 CALM1 CALM2 CALM3
42 11.12 CALM1 CALM2 CALM3
43 10.98 CALM1 CALM2 CALM3
44 10.89 CALM1 CALM2 CALM3
45 10.86 CALM1 CALM2 CALM3
46 10.66 CALM1 CALM2 CALM3

GO Terms for Primary Cutaneous Amyloidosis

Cellular components related to Primary Cutaneous Amyloidosis according to GeneCards Suite gene sharing:

id Name GO ID Score Top Affiliating Genes
1 keratin filament GO:0045095 9.55 KRT14 KRT18 KRT5 KRT7 KRT8
2 sarcomere GO:0030017 9.5 CALM1 CALM2 CALM3
3 calcium channel complex GO:0034704 9.43 CALM1 CALM2 CALM3
4 dystrophin-associated glycoprotein complex GO:0016010 9.4 KRT19 KRT8
5 cell periphery GO:0071944 9.35 KRT14 KRT17 KRT18 KRT19 KRT8
6 intermediate filament GO:0005882 9.28 KRT10 KRT14 KRT16 KRT17 KRT18 KRT19
7 extracellular exosome GO:0070062 10.07 KRT10 KRT14 KRT16 KRT17 KRT18 KRT19

Biological processes related to Primary Cutaneous Amyloidosis according to GeneCards Suite gene sharing:

(show all 25)
id Name GO ID Score Top Affiliating Genes
1 epidermis development GO:0008544 9.86 KRT14 KRT16 KRT17 KRT5
2 response to calcium ion GO:0051592 9.77 CALM1 CALM2 CALM3
3 positive regulation of protein serine/threonine kinase activity GO:0071902 9.76 CALM1 CALM2 CALM3
4 regulation of heart rate GO:0002027 9.75 CALM1 CALM2 CALM3
5 positive regulation of peptidyl-threonine phosphorylation GO:0010800 9.74 CALM1 CALM2 CALM3
6 positive regulation of protein dephosphorylation GO:0035307 9.72 CALM1 CALM2 CALM3
7 regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum GO:0010880 9.71 CALM1 CALM2 CALM3
8 positive regulation of protein autophosphorylation GO:0031954 9.7 CALM1 CALM2 CALM3
9 regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion GO:0010881 9.69 CALM1 CALM2 CALM3
10 regulation of cardiac muscle contraction GO:0055117 9.67 CALM1 CALM2 CALM3
11 negative regulation of peptidyl-threonine phosphorylation GO:0010801 9.65 CALM1 CALM2 CALM3
12 positive regulation of phosphoprotein phosphatase activity GO:0032516 9.63 CALM1 CALM2 CALM3
13 hair cycle GO:0042633 9.62 KRT14 KRT16
14 positive regulation of wound healing GO:0090303 9.62 CCL2 MYLK
15 hepatocyte apoptotic process GO:0097284 9.61 KRT18 KRT8
16 hemidesmosome assembly GO:0031581 9.61 KRT14 KRT5
17 detection of calcium ion GO:0005513 9.61 CALM1 CALM2 CALM3
18 keratinization GO:0031424 9.61 KRT10 KRT14 KRT16 KRT17 KRT18 KRT19
19 cell differentiation involved in embryonic placenta development GO:0060706 9.59 KRT19 KRT8
20 negative regulation of ryanodine-sensitive calcium-release channel activity GO:0060315 9.58 CALM1 CALM2 CALM3
21 positive regulation of ryanodine-sensitive calcium-release channel activity GO:0060316 9.54 CALM1 CALM2 CALM3
22 regulation of cell communication by electrical coupling involved in cardiac conduction GO:1901844 9.5 CALM1 CALM2 CALM3
23 positive regulation of cyclic-nucleotide phosphodiesterase activity GO:0051343 9.43 CALM1 CALM2 CALM3
24 positive regulation of cyclic nucleotide metabolic process GO:0030801 9.33 CALM1 CALM2 CALM3
25 cornification GO:0070268 9.28 KRT10 KRT14 KRT16 KRT17 KRT18 KRT19

Molecular functions related to Primary Cutaneous Amyloidosis according to GeneCards Suite gene sharing:

id Name GO ID Score Top Affiliating Genes
1 structural constituent of cytoskeleton GO:0005200 9.55 KRT14 KRT16 KRT17 KRT19 KRT5
2 scaffold protein binding GO:0097110 9.54 KRT18 KRT5 KRT8
3 protein serine/threonine kinase activator activity GO:0043539 9.5 CALM1 CALM2 CALM3
4 titin binding GO:0031432 9.43 CALM1 CALM2 CALM3
5 structural molecule activity GO:0005198 9.35 KRT16 KRT17 KRT18 KRT7 KRT8
6 protein phosphatase activator activity GO:0072542 8.8 CALM1 CALM2 CALM3

Sources for Primary Cutaneous Amyloidosis

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 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 MedGen
42 MeSH
43 MESH via Orphanet
44 MGI
46 NCI
47 NCIt
48 NDF-RT
51 NINDS
52 Novoseek
54 OMIM
55 OMIM via Orphanet
59 PubMed
60 QIAGEN
65 SNOMED-CT via HPO
66 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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