Home Contact Sitemap

eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   congenital hemolytic anemia
  

Disease ID 1010
Disease congenital hemolytic anemia
Definition
Hemolytic anemia due to various intrinsic defects of the erythrocyte.
Synonym
anaemia -heredit.haemol
anaemias haemolytics hereditary
anemia -heredit.hemol
anemia hemolytic congen
anemia, congenital hemolytic
anemia, hemolytic, congenital
anemia, hemolytic, congenital [disease/finding]
anemia, hemolytic, hereditary
anemia, hereditary hemolytic
anemias, congenital hemolytic
anemias, hereditary hemolytic
congen hemolytic anemia
congenital haemolytic anaemia
congenital haemolytic anemia
congenital hemolytic anemia (disorder)
congenital hemolytic anemia, nos
congenital hemolytic anemias
hemolytic anemia congen
hemolytic anemia, congenital
hemolytic anemia, hereditary
hemolytic anemias, congenital
hemolytic anemias, hereditary
hered hemolytic anem nos
hereditary haemol.anaem
hereditary haemolytic anaemia
hereditary haemolytic anaemia nos
hereditary haemolytic anaemias
hereditary hemol.anaem
hereditary hemolytic anemia
hereditary hemolytic anemia (disorder)
hereditary hemolytic anemia nos
hereditary hemolytic anemia nos (disorder)
hereditary hemolytic anemia, nos
hereditary hemolytic anemia, unspecified
hereditary hemolytic anemias
other hered. haem. anaemias
other hered. hem. anemias
DOID
ICD10
UMLS
C0002881
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:6)
C0002871  |  anaemia  |  1
C0398623  |  hypercoagulability  |  1
C0340968  |  pyruvate kinase deficiency  |  1
C0019045  |  haemoglobinopathies  |  1
C0039730  |  thalassemia  |  1
C0029106  |  opisthorchiasis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:33)
6521  |  SLC4A1  |  UniProtKB-KW;GHR
6708  |  SPTA1  |  UniProtKB-KW;GHR
5230  |  PGK1  |  UniProtKB-KW
9949  |  AMMECR1  |  UniProtKB-KW
203  |  AK1  |  UniProtKB-KW
669  |  BPGM  |  UniProtKB-KW
6005  |  RHAG  |  UniProtKB-KW
3039  |  HBA1  |  UniProtKB-KW
3040  |  HBA2  |  UniProtKB-KW
10483  |  SEC23B  |  UniProtKB-KW;GHR
100  |  ADA  |  UniProtKB-KW
2182  |  ACSL4  |  UniProtKB-KW
5313  |  PKLR  |  UniProtKB-KW
3043  |  HBB  |  UniProtKB-KW
6513  |  SLC2A1  |  UniProtKB-KW
6710  |  SPTB  |  UniProtKB-KW;GHR
226  |  ALDOA  |  UniProtKB-KW
2937  |  GSS  |  UniProtKB-KW
10661  |  KLF1  |  UniProtKB-KW
966  |  CD59  |  UniProtKB-KW
2539  |  G6PD  |  UniProtKB-KW
146059  |  CDAN1  |  UniProtKB-KW;GHR
286  |  ANK1  |  UniProtKB-KW;GHR
3783  |  KCNN4  |  UniProtKB-KW
2821  |  GPI  |  UniProtKB-KW
2035  |  EPB41  |  UniProtKB-KW
9780  |  PIEZO1  |  UniProtKB-KW
7167  |  TPI1  |  UniProtKB-KW
9663  |  LPIN2  |  UniProtKB-KW
6007  |  RHD  |  CTD_human
2038  |  EPB42  |  UniProtKB-KW;GHR
2729  |  GCLC  |  UniProtKB-KW
6006  |  RHCE  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:3)
2038  |  EPB42  |  CIPHER
6007  |  RHD  |  CTD_human
6006  |  RHCE  |  CTD_human
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:231)
55  |  ACPP  |  1.191  |  DISEASES
120  |  ADD3  |  2.197  |  DISEASES
203  |  AK1  |  1.464  |  DISEASES
212  |  ALAS2  |  1.306  |  DISEASES
226  |  ALDOA  |  1.512  |  DISEASES
287  |  ANK2  |  2.267  |  DISEASES
310  |  ANXA7  |  1.932  |  DISEASES
9070  |  ASH2L  |  1.15  |  DISEASES
54829  |  ASPN  |  1.204  |  DISEASES
286410  |  ATP11C  |  1.624  |  DISEASES
488  |  ATP2A2  |  1.16  |  DISEASES
10396  |  ATP8A1  |  1.691  |  DISEASES
7917  |  BAG6  |  1.16  |  DISEASES
29994  |  BAZ2B  |  1.063  |  DISEASES
53335  |  BCL11A  |  4.554  |  DISEASES
617  |  BCS1L  |  4.139  |  DISEASES
84529  |  C15orf41  |  2.76  |  DISEASES
25912  |  C1orf43  |  2.227  |  DISEASES
9254  |  CACNA2D2  |  1.081  |  DISEASES
51806  |  CALML5  |  1.63  |  DISEASES
831  |  CAST  |  1.002  |  DISEASES
11314  |  CD300A  |  1.523  |  DISEASES
951  |  CD37  |  1.303  |  DISEASES
958  |  CD40  |  1.25  |  DISEASES
959  |  CD40LG  |  2.785  |  DISEASES
960  |  CD44  |  1.771  |  DISEASES
961  |  CD47  |  3.075  |  DISEASES
921  |  CD5  |  1.314  |  DISEASES
922  |  CD5L  |  2.581  |  DISEASES
146059  |  CDAN1  |  5.521  |  DISEASES
988  |  CDC5L  |  1.029  |  DISEASES
26097  |  CHTOP  |  2.123  |  DISEASES
9635  |  CLCA2  |  2.415  |  DISEASES
22802  |  CLCA4  |  2.513  |  DISEASES
1192  |  CLIC1  |  2.76  |  DISEASES
54544  |  CRCT1  |  2.254  |  DISEASES
2017  |  CTTN  |  4.215  |  DISEASES
1523  |  CUX1  |  1.221  |  DISEASES
6387  |  CXCL12  |  1.253  |  DISEASES
7852  |  CXCR4  |  1.274  |  DISEASES
1528  |  CYB5A  |  4.52  |  DISEASES
51706  |  CYB5R1  |  4.055  |  DISEASES
1727  |  CYB5R3  |  5.543  |  DISEASES
51167  |  CYB5R4  |  3.729  |  DISEASES
1538  |  CYLC1  |  2.211  |  DISEASES
1539  |  CYLC2  |  1.96  |  DISEASES
260293  |  CYP4X1  |  2.172  |  DISEASES
27071  |  DAPP1  |  1.966  |  DISEASES
28988  |  DBNL  |  2.78  |  DISEASES
85458  |  DIXDC1  |  1.347  |  DISEASES
1785  |  DNM2  |  2.732  |  DISEASES
1786  |  DNMT1  |  1.435  |  DISEASES
1937  |  EEF1G  |  1.346  |  DISEASES
25975  |  EGFL6  |  1.437  |  DISEASES
1978  |  EIF4EBP1  |  1.095  |  DISEASES
284361  |  EMC10  |  3.378  |  DISEASES
953  |  ENTPD1  |  2.432  |  DISEASES
377841  |  ENTPD8  |  1.309  |  DISEASES
2035  |  EPB41  |  5.128  |  DISEASES
2135  |  EXTL2  |  1.519  |  DISEASES
2165  |  F13B  |  3.191  |  DISEASES
131177  |  FAM3D  |  2.128  |  DISEASES
2242  |  FES  |  1.18  |  DISEASES
2268  |  FGR  |  3.153  |  DISEASES
166752  |  FREM3  |  1.625  |  DISEASES
6624  |  FSCN1  |  1.772  |  DISEASES
2533  |  FYB  |  1.567  |  DISEASES
2534  |  FYN  |  2.783  |  DISEASES
2623  |  GATA1  |  5.275  |  DISEASES
2624  |  GATA2  |  2.46  |  DISEASES
85476  |  GFM1  |  1.575  |  DISEASES
2689  |  GH2  |  1.485  |  DISEASES
2821  |  GPI  |  2.368  |  DISEASES
26086  |  GPSM1  |  1.799  |  DISEASES
9402  |  GRAP2  |  1.257  |  DISEASES
2885  |  GRB2  |  1.708  |  DISEASES
2886  |  GRB7  |  1.341  |  DISEASES
2993  |  GYPA  |  4.104  |  DISEASES
2994  |  GYPB  |  2.83  |  DISEASES
2996  |  GYPE  |  1.062  |  DISEASES
3005  |  H1F0  |  3.116  |  DISEASES
10456  |  HAX1  |  5.263  |  DISEASES
3039  |  HBA1  |  3.459  |  DISEASES
3043  |  HBB  |  6.759  |  DISEASES
3045  |  HBD  |  5.82  |  DISEASES
3047  |  HBG1  |  5.275  |  DISEASES
3048  |  HBG2  |  4.086  |  DISEASES
10767  |  HBS1L  |  3.256  |  DISEASES
23462  |  HEY1  |  1.066  |  DISEASES
3077  |  HFE  |  2.006  |  DISEASES
148738  |  HFE2  |  1.08  |  DISEASES
8337  |  HIST2H2AA3  |  1.154  |  DISEASES
8338  |  HIST2H2AC  |  1.154  |  DISEASES
8349  |  HIST2H2BE  |  2.983  |  DISEASES
3240  |  HP  |  3.413  |  DISEASES
9653  |  HS2ST1  |  4.176  |  DISEASES
9953  |  HS3ST3B1  |  1.774  |  DISEASES
222537  |  HS3ST5  |  3.224  |  DISEASES
64711  |  HS3ST6  |  2.473  |  DISEASES
90161  |  HS6ST2  |  1.479  |  DISEASES
51182  |  HSPA14  |  1.285  |  DISEASES
3386  |  ICAM4  |  1.33  |  DISEASES
23463  |  ICMT  |  1.668  |  DISEASES
100423062  |  IGLL5  |  1.068  |  DISEASES
3608  |  ILF2  |  1.288  |  DISEASES
27152  |  INTU  |  1.405  |  DISEASES
3717  |  JAK2  |  1.05  |  DISEASES
3725  |  JUN  |  1.547  |  DISEASES
3767  |  KCNJ11  |  2.109  |  DISEASES
200845  |  KCTD6  |  2.697  |  DISEASES
23028  |  KDM1A  |  1.344  |  DISEASES
3792  |  KEL  |  1.595  |  DISEASES
3932  |  LCK  |  2.785  |  DISEASES
197021  |  LCTL  |  1.396  |  DISEASES
4067  |  LYN  |  4.013  |  DISEASES
23499  |  MACF1  |  1.076  |  DISEASES
4094  |  MAF  |  2.378  |  DISEASES
23764  |  MAFF  |  2.093  |  DISEASES
7975  |  MAFK  |  2.908  |  DISEASES
347541  |  MAGEB5  |  2.765  |  DISEASES
11184  |  MAP4K1  |  2.875  |  DISEASES
7867  |  MAPKAPK3  |  1.078  |  DISEASES
4151  |  MB  |  1.231  |  DISEASES
4170  |  MCL1  |  1.115  |  DISEASES
8972  |  MGAM  |  1.309  |  DISEASES
4248  |  MGAT3  |  1.534  |  DISEASES
284424  |  MIR7-3HG  |  1.245  |  DISEASES
4519  |  MT-CYB  |  2.083  |  DISEASES
389125  |  MUSTN1  |  1.812  |  DISEASES
4700  |  NDUFA6  |  1.285  |  DISEASES
91624  |  NEXN  |  1.91  |  DISEASES
4779  |  NFE2L1  |  2.229  |  DISEASES
58160  |  NFE4  |  3.234  |  DISEASES
4802  |  NFYC  |  1.328  |  DISEASES
9221  |  NOLC1  |  1.528  |  DISEASES
8131  |  NPRL3  |  4.515  |  DISEASES
140767  |  NRSN1  |  2.505  |  DISEASES
84033  |  OBSCN  |  1.118  |  DISEASES
283111  |  OR51V1  |  2.445  |  DISEASES
5079  |  PAX5  |  2.554  |  DISEASES
27328  |  PCDH11X  |  1.804  |  DISEASES
56147  |  PCDHA1  |  2.326  |  DISEASES
5110  |  PCMT1  |  2.332  |  DISEASES
10954  |  PDIA5  |  1.673  |  DISEASES
5213  |  PFKM  |  1.22  |  DISEASES
5313  |  PKLR  |  4.215  |  DISEASES
51177  |  PLEKHO1  |  2.321  |  DISEASES
5440  |  POLR2K  |  2.386  |  DISEASES
5441  |  POLR2L  |  2.383  |  DISEASES
5450  |  POU2AF1  |  2.141  |  DISEASES
56342  |  PPAN  |  1.545  |  DISEASES
84919  |  PPP1R15B  |  1.657  |  DISEASES
56980  |  PRDM10  |  1.033  |  DISEASES
5592  |  PRKG1  |  1.537  |  DISEASES
5634  |  PRPS2  |  1.011  |  DISEASES
5710  |  PSMD4  |  2.423  |  DISEASES
9050  |  PSTPIP2  |  1.371  |  DISEASES
5788  |  PTPRC  |  1.9  |  DISEASES
55278  |  QRSL1  |  1.39  |  DISEASES
8437  |  RASAL1  |  1.021  |  DISEASES
23029  |  RBM34  |  3.095  |  DISEASES
6005  |  RHAG  |  3.389  |  DISEASES
6007  |  RHD  |  1.343  |  DISEASES
56254  |  RNF20  |  1.306  |  DISEASES
4919  |  ROR1  |  1.229  |  DISEASES
6139  |  RPL17  |  2.428  |  DISEASES
6207  |  RPS13  |  2.782  |  DISEASES
6209  |  RPS15  |  1.97  |  DISEASES
6222  |  RPS18  |  1.07  |  DISEASES
6223  |  RPS19  |  2.338  |  DISEASES
6224  |  RPS20  |  1.26  |  DISEASES
6227  |  RPS21  |  2.675  |  DISEASES
6230  |  RPS25  |  2.249  |  DISEASES
6231  |  RPS26  |  1.966  |  DISEASES
6188  |  RPS3  |  3.512  |  DISEASES
6189  |  RPS3A  |  5.257  |  DISEASES
338324  |  S100A7A  |  1.928  |  DISEASES
22908  |  SACM1L  |  1.297  |  DISEASES
6304  |  SATB1  |  1.809  |  DISEASES
60485  |  SAV1  |  1.867  |  DISEASES
388228  |  SBK1  |  1.6  |  DISEASES
462  |  SERPINC1  |  2.235  |  DISEASES
29072  |  SETD2  |  1.405  |  DISEASES
253970  |  SFTA3  |  3.393  |  DISEASES
729238  |  SFTPA2  |  1.317  |  DISEASES
30011  |  SH3KBP1  |  1.19  |  DISEASES
6461  |  SHB  |  3.2  |  DISEASES
51312  |  SLC25A37  |  1.193  |  DISEASES
65010  |  SLC26A6  |  1.768  |  DISEASES
116369  |  SLC26A8  |  2.772  |  DISEASES
83650  |  SLC35G5  |  2.474  |  DISEASES
6522  |  SLC4A2  |  1.236  |  DISEASES
6533  |  SLC6A6  |  1.516  |  DISEASES
133308  |  SLC9B2  |  1.719  |  DISEASES
6597  |  SMARCA4  |  1.073  |  DISEASES
6605  |  SMARCE1  |  1.005  |  DISEASES
9301  |  SNORD27  |  1.381  |  DISEASES
6654  |  SOS1  |  1.264  |  DISEASES
55553  |  SOX6  |  2.788  |  DISEASES
6708  |  SPTA1  |  4.887  |  DISEASES
6710  |  SPTB  |  4.174  |  DISEASES
10011  |  SRA1  |  1.172  |  DISEASES
6714  |  SRC  |  3.031  |  DISEASES
6744  |  SSFA2  |  1.779  |  DISEASES
8428  |  STK24  |  1.229  |  DISEASES
161497  |  STRC  |  1.167  |  DISEASES
25777  |  SUN2  |  1.18  |  DISEASES
6850  |  SYK  |  3.113  |  DISEASES
83860  |  TAF3  |  2.576  |  DISEASES
6877  |  TAF5  |  2.268  |  DISEASES
7018  |  TF  |  2.98  |  DISEASES
7037  |  TFRC  |  2.75  |  DISEASES
7091  |  TLE4  |  1.09  |  DISEASES
7124  |  TNF  |  1.16  |  DISEASES
25987  |  TSKU  |  1.155  |  DISEASES
7318  |  UBA7  |  2.141  |  DISEASES
9898  |  UBAP2L  |  1.956  |  DISEASES
7391  |  USF1  |  2.078  |  DISEASES
10090  |  UST  |  2.671  |  DISEASES
7409  |  VAV1  |  3.522  |  DISEASES
7716  |  VEZF1  |  2.032  |  DISEASES
7454  |  WAS  |  2.192  |  DISEASES
10163  |  WASF2  |  1.373  |  DISEASES
23038  |  WDTC1  |  1.27  |  DISEASES
56949  |  XAB2  |  1.683  |  DISEASES
9213  |  XPR1  |  1.743  |  DISEASES
404281  |  YY2  |  2.255  |  DISEASES
51341  |  ZBTB7A  |  1.467  |  DISEASES
161882  |  ZFPM1  |  1.382  |  DISEASES
10782  |  ZNF274  |  1.494  |  DISEASES
283337  |  ZNF740  |  1.515  |  DISEASES
Locus(Waiting for update.)
Disease ID 1010
Disease congenital hemolytic anemia
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:4)
HP:0001903  |  Anemia  |  1
HP:0001744  |  Splenomegaly  |  1
HP:0100724  |  Hypercoagulability  |  1
HP:0001250  |  Seizures  |  1
Disease ID 1010
Disease congenital hemolytic anemia
Manually Symptom
UMLS  | Name(Total Manually Symptoms:5)
C2203646  |  jaundice
C1963148  |  iron overload
C1961102  |  acute lymphoblastic leukemia
C0023449  |  acute lymphoblastic leukaemia
C0017926  |  phosphofructokinase deficiency
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Disease ID 1010
Disease congenital hemolytic anemia
Case(Waiting for update.)