CMD1CC
MCID: CRD115
MIFTS: 23

Cardiomyopathy, Dilated, 1cc (CMD1CC)

Categories: Blood diseases, Bone diseases, Cardiovascular diseases, Ear diseases, Genetic diseases, Immune diseases, Neuronal diseases, Rare diseases, Respiratory diseases

Aliases & Classifications for Cardiomyopathy, Dilated, 1cc

MalaCards integrated aliases for Cardiomyopathy, Dilated, 1cc:

Name: Cardiomyopathy, Dilated, 1cc 56 13 71
Dilated Cardiomyopathy 1cc 12 29 6
Cmd1cc 56 12 73
Cardiomyopathy, Dilated, Type 1cc 39
Cardiomyopathy, Dilated 1cc 73

Characteristics:

OMIM:

56
Inheritance:
autosomal dominant

Miscellaneous:
average age of onset 50.8 +/- 9.0 years
some patients require cardiac transplantation


HPO:

31
cardiomyopathy, dilated, 1cc:
Inheritance autosomal dominant inheritance


Classifications:



External Ids:

Disease Ontology 12 DOID:0110424
OMIM 56 613122
OMIM Phenotypic Series 56 PS115200
MeSH 43 D002311
ICD10 32 I42.0
MedGen 41 C2751084
SNOMED-CT via HPO 68 195021004 263681008 399020009
UMLS 71 C2751084

Summaries for Cardiomyopathy, Dilated, 1cc

UniProtKB/Swiss-Prot : 73 Cardiomyopathy, dilated 1CC: A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death.

MalaCards based summary : Cardiomyopathy, Dilated, 1cc, is also known as dilated cardiomyopathy 1cc. An important gene associated with Cardiomyopathy, Dilated, 1cc is NEXN (Nexilin F-Actin Binding Protein). Affiliated tissues include heart, and related phenotype is dilated cardiomyopathy.

Disease Ontology : 12 A dilated cardiomyopathy that has material basis in mutation in the NEXN gene on chromosome 1p31.1.

More information from OMIM: 613122 PS115200

Symptoms & Phenotypes for Cardiomyopathy, Dilated, 1cc

Human phenotypes related to Cardiomyopathy, Dilated, 1cc:

31 (showing 1, show less)
# Description HPO Frequency HPO Source Accession
1 dilated cardiomyopathy 31 HP:0001644

Symptoms via clinical synopsis from OMIM:

56
Cardiovascular Heart:
cardiomyopathy, dilated
decreased left ventricular ejection fraction
decreased left ventricular end diastolic diameter

Clinical features from OMIM:

613122

Drugs & Therapeutics for Cardiomyopathy, Dilated, 1cc

Search Clinical Trials , NIH Clinical Center for Cardiomyopathy, Dilated, 1cc

Genetic Tests for Cardiomyopathy, Dilated, 1cc

Genetic tests related to Cardiomyopathy, Dilated, 1cc:

# Genetic test Affiliating Genes
1 Dilated Cardiomyopathy 1cc 29 NEXN

Anatomical Context for Cardiomyopathy, Dilated, 1cc

MalaCards organs/tissues related to Cardiomyopathy, Dilated, 1cc:

40
Heart

Publications for Cardiomyopathy, Dilated, 1cc

Articles related to Cardiomyopathy, Dilated, 1cc:

(showing 2, show less)
# Title Authors PMID Year
1
Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy. 56 6
19881492 2009
2
Dilated Cardiomyopathy Overview 6
20301486 2007

Variations for Cardiomyopathy, Dilated, 1cc

ClinVar genetic disease variations for Cardiomyopathy, Dilated, 1cc:

6 (showing 104, show less) ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎ ‎‎
# Gene Name Type Significance ClinVarId dbSNP ID GRCh37 Pos GRCh38 Pos
1 NEXN NEXN, 3-BP DEL, 1948GGAdeletion Pathogenic 325
2 NEXN NM_144573.3(NEXN):c.1831C>A (p.Pro611Thr)SNV Pathogenic 327 rs137853198 1:78408317-78408317 1:77942632-77942632
3 NEXN NM_144573.3(NEXN):c.799G>T (p.Glu267Ter)SNV Likely pathogenic 599095 rs771262904 1:78392512-78392512 1:77926827-77926827
4 NEXN NM_144573.4(NEXN):c.835C>T (p.Arg279Cys)SNV Conflicting interpretations of pathogenicity 30994 rs146245480 1:78392548-78392548 1:77926863-77926863
5 NEXN NM_144573.4(NEXN):c.1955A>G (p.Tyr652Cys)SNV Conflicting interpretations of pathogenicity 326 rs137853197 1:78408441-78408441 1:77942756-77942756
6 NEXN NM_144573.3(NEXN):c.1918_1922del (p.Tyr640fs)deletion Conflicting interpretations of pathogenicity 470680 rs1222794437 1:78408401-78408405 1:77942716-77942720
7 NEXN NM_144573.3(NEXN):c.1671_1673GGA[2] (p.Glu561_Glu562del)short repeat Conflicting interpretations of pathogenicity 47893 rs397517848 1:78408155-78408160 1:77942470-77942475
8 NEXN NM_144573.4(NEXN):c.1946_1948GAG[1] (p.Gly650del)short repeat Conflicting interpretations of pathogenicity 47899 rs397517853 1:78408435-78408437 1:77942746-77942748
9 NEXN NM_144573.4(NEXN):c.732C>A (p.Pro244=)SNV Conflicting interpretations of pathogenicity 47910 rs201171783 1:78392445-78392445 1:77926760-77926760
10 NEXN NM_144573.4(NEXN):c.893C>G (p.Thr298Arg)SNV Conflicting interpretations of pathogenicity 47914 rs200753280 1:78395029-78395029 1:77929344-77929344
11 NEXN NM_144573.4(NEXN):c.995A>C (p.Glu332Ala)SNV Conflicting interpretations of pathogenicity 47915 rs201763096 1:78395131-78395131 1:77929446-77929446
12 NEXN NM_144573.4(NEXN):c.1408G>C (p.Glu470Gln)SNV Conflicting interpretations of pathogenicity 138511 rs35366555 1:78401664-78401664 1:77935979-77935979
13 NEXN NM_144573.4(NEXN):c.1252-10T>GSNV Conflicting interpretations of pathogenicity 178878 rs201019553 1:78401498-78401498 1:77935813-77935813
14 NEXN NM_144573.4(NEXN):c.249G>A (p.Glu83=)SNV Conflicting interpretations of pathogenicity 178102 rs372532824 1:78383674-78383674 1:77917989-77917989
15 NEXN NM_144573.4(NEXN):c.949A>C (p.Met317Leu)SNV Conflicting interpretations of pathogenicity 178904 rs559464457 1:78395085-78395085 1:77929400-77929400
16 NEXN NM_144573.4(NEXN):c.1029G>A (p.Ala343=)SNV Conflicting interpretations of pathogenicity 178103 rs374260457 1:78395165-78395165 1:77929480-77929480
17 NEXN NM_144573.4(NEXN):c.512T>C (p.Ile171Thr)SNV Conflicting interpretations of pathogenicity 201917 rs372065024 1:78392121-78392121 1:77926436-77926436
18 NEXN NM_144573.3(NEXN):c.856C>T (p.Arg286Trp)SNV Conflicting interpretations of pathogenicity 201919 rs199917913 1:78392569-78392569 1:77926884-77926884
19 NEXN NM_001172309.1(NEXN):c.1479_1481GGA[3] (p.Glu498del)short repeat Conflicting interpretations of pathogenicity 201945 rs397517848 1:78408155-78408157 1:77942470-77942472
20 NEXN NM_144573.3(NEXN):c.2026_*1deldeletion Uncertain significance 201946 rs794729094 1:78408509-78408512 1:77942824-77942827
21 NEXN NM_144573.4(NEXN):c.86G>T (p.Gly29Val)SNV Uncertain significance 229061 rs876657931 1:78383309-78383309 1:77917624-77917624
22 NEXN NM_144573.3(NEXN):c.1572_1574delAGAshort repeat Uncertain significance 194130 rs764505909 1:78407806-78407808 1:77942121-77942123
23 NEXN NM_144573.3(NEXN):c.242A>T (p.Asp81Val)SNV Uncertain significance 201915 rs367871780 1:78383667-78383667 1:77917982-77917982
24 NEXN NM_144573.4(NEXN):c.613G>A (p.Glu205Lys)SNV Uncertain significance 47908 rs201447781 1:78392222-78392222 1:77926537-77926537
25 NEXN NM_144573.3(NEXN):c.1640T>C (p.Ile547Thr)SNV Uncertain significance 201944 rs753636624 1:78407874-78407874 1:77942189-77942189
26 NEXN NM_144573.4(NEXN):c.379C>T (p.Arg127Cys)SNV Uncertain significance 229058 rs771113424 1:78383890-78383890 1:77918205-77918205
27 NEXN NM_144573.4(NEXN):c.1174C>T (p.Arg392Ter)SNV Uncertain significance 229051 rs750076188 1:78399087-78399087 1:77933402-77933402
28 NEXN NM_144573.4(NEXN):c.1415C>G (p.Ala472Gly)SNV Uncertain significance 229054 rs539665448 1:78401671-78401671 1:77935986-77935986
29 NEXN NM_144573.3(NEXN):c.1820_1822del (p.Gly607del)deletion Uncertain significance 229055 rs876657928 1:78408304-78408306 1:77942619-77942621
30 NEXN NM_144573.3(NEXN):c.687+4A>TSNV Uncertain significance 241866 rs754061340 1:78392300-78392300 1:77926615-77926615
31 NEXN NM_144573.3(NEXN):c.392A>C (p.Gln131Pro)SNV Uncertain significance 264597 rs397517858 1:78383903-78383903 1:77918218-77918218
32 NEXN NM_144573.3(NEXN):c.671G>A (p.Cys224Tyr)SNV Uncertain significance 298088 rs886046534 1:78392280-78392280 1:77926595-77926595
33 NEXN NM_144573.3(NEXN):c.1271C>T (p.Thr424Ile)SNV Uncertain significance 201924 rs200442502 1:78401527-78401527 1:77935842-77935842
34 NEXN NM_144573.3(NEXN):c.1416_1418AAG[1] (p.Arg475del)short repeat Uncertain significance 201940 rs794729091 1:78401672-78401674 1:77935987-77935989
35 NEXN NM_144573.3(NEXN):c.1430T>C (p.Ile477Thr)SNV Uncertain significance 201934 rs727504658 1:78401686-78401686 1:77936001-77936001
36 NEXN NM_144573.3(NEXN):c.1435C>T (p.Leu479Phe)SNV Uncertain significance 201925 rs181520023 1:78401691-78401691 1:77936006-77936006
37 NEXN NM_144573.3(NEXN):c.1471G>C (p.Glu491Gln)SNV Uncertain significance 201926 rs373057251 1:78401727-78401727 1:77936042-77936042
38 NEXN NM_144573.4(NEXN):c.1528A>G (p.Lys510Glu)SNV Uncertain significance 179277 rs727504758 1:78407762-78407762 1:77942077-77942077
39 NEXN NM_144573.4(NEXN):c.586C>T (p.Arg196Cys)SNV Uncertain significance 179003 rs369486891 1:78392195-78392195 1:77926510-77926510
40 NEXN NM_001172309.1(NEXN):c.1561_1563AAG[1] (p.Lys522del)short repeat Uncertain significance 47896 rs397517851 1:78408239-78408241 1:77942554-77942556
41 NEXN NM_144573.4(NEXN):c.1788T>G (p.Ser596Arg)SNV Uncertain significance 47897 rs199738750 1:78408274-78408274 1:77942589-77942589
42 NEXN NM_144573.3(NEXN):c.277G>C (p.Ala93Pro)SNV Uncertain significance 470682 rs1256690084 1:78383702-78383702 1:77918017-77918017
43 NEXN NM_144573.4(NEXN):c.1053+1G>ASNV Uncertain significance 47886 rs397517843 1:78395190-78395190 1:77929505-77929505
44 NEXN NM_144573.4(NEXN):c.1112C>T (p.Pro371Leu)SNV Uncertain significance 47887 rs200067011 1:78399025-78399025 1:77933340-77933340
45 NEXN NM_144573.4(NEXN):c.1401_1403AGA[2] (p.Glu470del)short repeat Uncertain significance 47890 rs397517846 1:78401657-78401659 1:77935972-77935974
46 NEXN NM_144573.4(NEXN):c.1453G>A (p.Glu485Lys)SNV Uncertain significance 47891 rs368812830 1:78401709-78401709 1:77936024-77936024
47 NEXN NM_144573.4(NEXN):c.1457C>G (p.Ala486Gly)SNV Uncertain significance 47892 rs397517847 1:78401713-78401713 1:77936028-77936028
48 NEXN NM_144573.3(NEXN):c.134G>T (p.Arg45Ile)SNV Uncertain significance 643060 1:78383357-78383357 1:77917672-77917672
49 NEXN NM_144573.3(NEXN):c.431C>T (p.Ala144Val)SNV Uncertain significance 662564 1:78383942-78383942 1:77918257-77918257
50 NEXN NM_144573.3(NEXN):c.542C>T (p.Thr181Ile)SNV Uncertain significance 661519 1:78392151-78392151 1:77926466-77926466
51 NEXN NM_144573.3(NEXN):c.857G>A (p.Arg286Gln)SNV Uncertain significance 645036 1:78392570-78392570 1:77926885-77926885
52 NEXN NM_144573.3(NEXN):c.1046G>C (p.Arg349Thr)SNV Uncertain significance 649140 1:78395182-78395182 1:77929497-77929497
53 NEXN NM_144573.3(NEXN):c.1055T>C (p.Val352Ala)SNV Uncertain significance 662435 1:78398968-78398968 1:77933283-77933283
54 NEXN NM_144573.3(NEXN):c.1697T>C (p.Met566Thr)SNV Uncertain significance 641866 1:78408183-78408183 1:77942498-77942498
55 NEXN NM_144573.3(NEXN):c.1739G>A (p.Gly580Glu)SNV Uncertain significance 664341 1:78408225-78408225 1:77942540-77942540
56 NEXN NM_144573.3(NEXN):c.1877A>G (p.Glu626Gly)SNV Uncertain significance 665536 1:78408363-78408363 1:77942678-77942678
57 NEXN NM_144573.3(NEXN):c.2008A>T (p.Thr670Ser)SNV Uncertain significance 658474 1:78408494-78408494 1:77942809-77942809
58 NEXN NM_144573.3(NEXN):c.818G>A (p.Arg273His)SNV Uncertain significance 538110 rs765385072 1:78392531-78392531 1:77926846-77926846
59 NEXN NM_144573.3(NEXN):c.1244T>C (p.Met415Thr)SNV Uncertain significance 538108 rs1172366391 1:78399157-78399157 1:77933472-77933472
60 NEXN NM_144573.3(NEXN):c.643C>G (p.Gln215Glu)SNV Uncertain significance 569703 rs1557981819 1:78392252-78392252 1:77926567-77926567
61 NEXN NM_144573.3(NEXN):c.752T>G (p.Phe251Cys)SNV Uncertain significance 575147 rs554389574 1:78392465-78392465 1:77926780-77926780
62 NEXN NM_144573.3(NEXN):c.250G>A (p.Glu84Lys)SNV Uncertain significance 582416 rs547319928 1:78383675-78383675 1:77917990-77917990
63 NEXN NM_144573.3(NEXN):c.1664_1666del (p.Arg555_Glu556delinsLys)deletion Uncertain significance 575564 rs1221963637 1:78408150-78408152 1:77942465-77942467
64 NEXN NC_000001.11:g.(?_77933272)_(77936054_?)dupduplication Uncertain significance 831977 1:78398957-78401739
65 NEXN NM_144573.4(NEXN):c.55C>T (p.Pro19Ser)SNV Uncertain significance 835184 1:78383278-78383278 1:77917593-77917593
66 NEXN NM_144573.4(NEXN):c.848A>T (p.Glu283Val)SNV Uncertain significance 855801 1:78392561-78392561 1:77926876-77926876
67 NEXN NM_144573.4(NEXN):c.1451G>A (p.Arg484Gln)SNV Uncertain significance 838951 1:78401707-78401707 1:77936022-77936022
68 NEXN NM_144573.4(NEXN):c.1928A>C (p.Glu643Ala)SNV Uncertain significance 848721 1:78408414-78408414 1:77942729-77942729
69 NEXN NM_144573.4(NEXN):c.2014G>A (p.Glu672Lys)SNV Uncertain significance 841719 1:78408500-78408500 1:77942815-77942815
70 NEXN NM_144573.4(NEXN):c.1473+1G>TSNV Uncertain significance 858417 1:78401730-78401730 1:77936045-77936045
71 NEXN NM_144573.3(NEXN):c.902T>A (p.Ile301Asn)SNV Uncertain significance 409281 rs373878384 1:78395038-78395038 1:77929353-77929353
72 NEXN NM_144573.3(NEXN):c.1852G>A (p.Glu618Lys)SNV Uncertain significance 409282 rs1060502321 1:78408338-78408338 1:77942653-77942653
73 NEXN NM_144573.3(NEXN):c.1687G>T (p.Gly563Cys)SNV Uncertain significance 417868 rs1060499571 1:78408173-78408173 1:77942488-77942488
74 NEXN NM_144573.3(NEXN):c.680T>C (p.Leu227Ser)SNV Uncertain significance 431969 rs756273801 1:78392289-78392289 1:77926604-77926604
75 NEXN NM_144573.3(NEXN):c.871G>A (p.Glu291Lys)SNV Uncertain significance 470684 rs770120245 1:78395007-78395007 1:77929322-77929322
76 NEXN NM_144573.3(NEXN):c.1429A>G (p.Ile477Val)SNV Uncertain significance 470678 rs1553240667 1:78401685-78401685 1:77936000-77936000
77 NEXN NM_144573.3(NEXN):c.1997C>A (p.Thr666Asn)SNV Uncertain significance 470681 rs749271412 1:78408483-78408483 1:77942798-77942798
78 NEXN NM_144573.3(NEXN):c.157G>A (p.Glu53Lys)SNV Uncertain significance 519153 rs373778361 1:78383380-78383380 1:77917695-77917695
79 NEXN NM_144573.3(NEXN):c.626G>T (p.Arg209Ile)SNV Uncertain significance 518919 rs1433269866 1:78392235-78392235 1:77926550-77926550
80 NEXN NM_144573.3(NEXN):c.1432G>A (p.Asp478Asn)SNV Uncertain significance 520368 rs1309129145 1:78401688-78401688 1:77936003-77936003
81 NEXN NM_144573.3(NEXN):c.1994G>T (p.Ser665Ile)SNV Uncertain significance 538111 rs777703689 1:78408480-78408480 1:77942795-77942795
82 NEXN NM_144573.3(NEXN):c.491A>G (p.Glu164Gly)SNV Uncertain significance 538106 rs1553238441 1:78392100-78392100 1:77926415-77926415
83 NEXN NM_144573.3(NEXN):c.767G>A (p.Arg256Gln)SNV Uncertain significance 538105 rs748921688 1:78392480-78392480 1:77926795-77926795
84 NEXN NM_144573.3(NEXN):c.1348dup (p.Ser450fs)duplication Uncertain significance 538107 rs1553240600 1:78401599-78401600 1:77935914-77935915
85 NEXN NM_001172309.1(NEXN):c.1709_1712delinsTCT (p.Gly570fs)indel Uncertain significance 538109 rs1553242300 1:78408387-78408390 1:77942702-77942705
86 NEXN NM_144573.3(NEXN):c.299-10A>GSNV Likely benign 538113 rs1452768769 1:78383800-78383800 1:77918115-77918115
87 NEXN NM_144573.3(NEXN):c.507A>G (p.Leu169=)SNV Likely benign 538112 rs776106290 1:78392116-78392116 1:77926431-77926431
88 NEXN NM_144573.3(NEXN):c.321T>A (p.Ala107=)SNV Likely benign 538114 rs1553236762 1:78383832-78383832 1:77918147-77918147
89 NEXN NM_144573.3(NEXN):c.1743T>G (p.Ala581=)SNV Likely benign 470679 rs772313224 1:78408229-78408229 1:77942544-77942544
90 NEXN NM_144573.3(NEXN):c.865-9T>CSNV Likely benign 695265 1:78394992-78394992 1:77929307-77929307
91 NEXN NM_144573.3(NEXN):c.1450C>A (p.Arg484=)SNV Likely benign 699510 1:78401706-78401706 1:77936021-77936021
92 NEXN NM_144573.3(NEXN):c.1401A>T (p.Ile467=)SNV Likely benign 744107 1:78401657-78401657 1:77935972-77935972
93 NEXN NM_144573.3(NEXN):c.66T>C (p.Tyr22=)SNV Likely benign 756867 1:78383289-78383289 1:77917604-77917604
94 NEXN NM_144573.3(NEXN):c.1137A>G (p.Glu379=)SNV Likely benign 470676 rs1553240026 1:78399050-78399050 1:77933365-77933365
95 NEXN NM_144573.4(NEXN):c.1704C>T (p.Gly568=)SNV Likely benign 47895 rs397517850 1:78408190-78408190 1:77942505-77942505
96 NEXN NM_144573.3(NEXN):c.1582G>C (p.Glu528Gln)SNV Likely benign 180456 rs200071700 1:78407816-78407816 1:77942131-77942131
97 NEXN NM_144573.3(NEXN):c.222T>C (p.Ile74=)SNV Likely benign 241865 rs767610015 1:78383647-78383647 1:77917962-77917962
98 NEXN NM_144573.4(NEXN):c.1785C>T (p.Asp595=)SNV Benign/Likely benign 264504 rs182998780 1:78408271-78408271 1:77942586-77942586
99 NEXN NM_144573.4(NEXN):c.156C>T (p.Asp52=)SNV Benign/Likely benign 226849 rs371431782 1:78383379-78383379 1:77917694-77917694
100 NEXN NM_144573.4(NEXN):c.1618A>G (p.Met540Val)SNV Benign/Likely benign 201929 rs201390657 1:78407852-78407852 1:77942167-77942167
101 NEXN NM_144573.4(NEXN):c.733G>A (p.Gly245Arg)SNV Benign/Likely benign 47911 rs1166698 1:78392446-78392446 1:77926761-77926761
102 NEXN NM_144573.4(NEXN):c.777A>G (p.Gln259=)SNV Benign/Likely benign 47912 rs375544798 1:78392490-78392490 1:77926805-77926805
103 NEXN NM_144573.4(NEXN):c.363G>A (p.Thr121=)SNV Benign/Likely benign 47906 rs35117963 1:78383874-78383874 1:77918189-77918189
104 NEXN NM_144573.3(NEXN):c.78T>C (p.Leu26=)SNV Benign/Likely benign 470683 rs376535223 1:78383301-78383301 1:77917616-77917616

UniProtKB/Swiss-Prot genetic disease variations for Cardiomyopathy, Dilated, 1cc:

73 (showing 2, show less)
# Symbol AA change Variation ID SNP ID
1 NEXN p.Pro611Thr VAR_063009 rs137853198
2 NEXN p.Tyr652Cys VAR_063011 rs137853197

Expression for Cardiomyopathy, Dilated, 1cc

Search GEO for disease gene expression data for Cardiomyopathy, Dilated, 1cc.

Pathways for Cardiomyopathy, Dilated, 1cc

GO Terms for Cardiomyopathy, Dilated, 1cc

Sources for Cardiomyopathy, Dilated, 1cc

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
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