PedAM

Pediatric Disease Annotations & Medicines


	pure red-cell aplasia

Disease ID	470
Disease	pure red-cell aplasia
Definition	Suppression of erythropoiesis with little or no abnormality of leukocyte or platelet production.
Synonym	aplasia cells pure red aplasia pure red cell aplasia, erythrocyte aplasia, pure red cell aplasia, pure red-cell aplasias, erythrocyte aplasias, pure red-cell erythrocyte aplasia erythrocyte aplasias primary red cell aplasia pure red cell anaemia pure red cell anemia pure red cell anemia, nos pure red cell aplasia pure red cell aplasia (disorder) pure red cell aplasia, nos pure red-cell aplasias red cell aplasia red cell aplasia nos red cell aplasia, pure red cell hypoplasia red-cell aplasia, pure red-cell aplasia, pure [disease/finding] red-cell aplasias, pure
Orphanet	ORPHANET:98421
DOID	DOID:1340
UMLS	C0034902
MeSH	D012010
SNOMED-CT	SNOMEDCT_US_2016_09_01:50715003
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:2) C0002878 \| hemolytic anemia \| 1 C0002871 \| anemia \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	Entrez_id \| Symbol \| Resource(Total Genes:2) 3105 \| HLA-A \| infer 3123 \| HLA-DRB1 \| infer
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:89) 920 \| CD4 \| DISEASES 6820 \| SULT2B1 \| DISEASES 3036 \| HAS1 \| DISEASES 2057 \| EPOR \| DISEASES 8288 \| EPX \| DISEASES 6143 \| RPL19 \| DISEASES 1440 \| CSF3 \| DISEASES 3558 \| IL2 \| DISEASES 92 \| ACVR2A \| DISEASES 1088 \| CEACAM8 \| DISEASES 79733 \| E2F8 \| DISEASES 6192 \| RPS4Y1 \| DISEASES 4695 \| NDUFA2 \| DISEASES 25873 \| RPL36 \| DISEASES 2056 \| EPO \| DISEASES 6155 \| RPL27 \| DISEASES 26122 \| EPC2 \| DISEASES 2995 \| GYPC \| DISEASES 11224 \| RPL35 \| DISEASES 3442 \| IFNA5 \| DISEASES 6132 \| RPL8 \| DISEASES 51816 \| CECR1 \| DISEASES 23523 \| CABIN1 \| DISEASES 6774 \| STAT3 \| DISEASES 7157 \| TP53 \| DISEASES 3930 \| LBR \| DISEASES 6233 \| RPS27A \| DISEASES 6567 \| SLC16A2 \| DISEASES 3439 \| IFNA1 \| DISEASES 925 \| CD8A \| DISEASES 27163 \| NAAA \| DISEASES 3889 \| KRT83 \| DISEASES 6154 \| RPL26 \| DISEASES 6006 \| RHCE \| DISEASES 2215 \| FCGR3B \| DISEASES 213 \| ALB \| DISEASES 3562 \| IL3 \| DISEASES 133418 \| EMB \| DISEASES 7314 \| UBB \| DISEASES 27087 \| B3GAT1 \| DISEASES 947 \| CD34 \| DISEASES 2523 \| FUT1 \| DISEASES 2824 \| GPM6B \| DISEASES 4684 \| NCAM1 \| DISEASES 10938 \| EHD1 \| DISEASES 6181 \| RPLP2 \| DISEASES 940 \| CD28 \| DISEASES 3824 \| KLRD1 \| DISEASES 6129 \| RPL7 \| DISEASES 921 \| CD5 \| DISEASES 9045 \| RPL14 \| DISEASES 6227 \| RPS21 \| DISEASES 6122 \| RPL3 \| DISEASES 6166 \| RPL36AL \| DISEASES 6218 \| RPS17 \| DISEASES 6189 \| RPS3A \| DISEASES 3240 \| HP \| DISEASES 2996 \| GYPE \| DISEASES 3821 \| KLRC1 \| DISEASES 2993 \| GYPA \| DISEASES 6170 \| RPL39 \| DISEASES 28982 \| FLVCR1 \| DISEASES 2214 \| FCGR3A \| DISEASES 284486 \| THEM5 \| DISEASES 914 \| CD2 \| DISEASES 6125 \| RPL5 \| DISEASES 959 \| CD40LG \| DISEASES 6191 \| RPS4X \| DISEASES 1043 \| CD52 \| DISEASES 6135 \| RPL11 \| DISEASES 3133 \| HLA-E \| DISEASES 1874 \| E2F4 \| DISEASES 54790 \| TET2 \| DISEASES 1876 \| E2F6 \| DISEASES 7018 \| TF \| DISEASES 55777 \| MBD5 \| DISEASES 1363 \| CPE \| DISEASES 7311 \| UBA52 \| DISEASES 6147 \| RPL23A \| DISEASES 3800 \| KIF5C \| DISEASES 6165 \| RPL35A \| DISEASES 1875 \| E2F5 \| DISEASES 6173 \| RPL36A \| DISEASES 6229 \| RPS24 \| DISEASES 26137 \| ZBTB20 \| DISEASES 51428 \| DDX41 \| DISEASES 6209 \| RPS15 \| DISEASES 6223 \| RPS19 \| DISEASES 100302740 \| FAS-AS1 \| DISEASES
Locus	(Waiting for update.)

Disease ID	470
Disease	pure red-cell aplasia
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:2) HP:0001878 \| Haemolytic anaemia \| 1 HP:0001903 \| Anemia \| 1

Disease ID	470
Disease	pure red-cell aplasia
Manually Symptom	UMLS \| Name(Total Manually Symptoms:2) C1420725 \| thymoma C1000483 \| anemia
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:1) C0002871 \| anemia \| 1

Manually Genotype(Total Text Mining 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.)

Chemical(Total Drugs:9)
CUI	ChemicalName	ChemicalID	CasRN	DiseaseName	DiseaseID	DirectEvidence	PubMedIDs
C0034902	ampicillin	D000667	69-53-4	red-cell aplasia, pure	MESH:D012010	marker/mechanism	2116345
C0034902	carbamazepine	D002220	298-46-4	red-cell aplasia, pure	MESH:D012010	marker/mechanism	12152855
C0034902	fenoprofen	D005279	31879-05-7	red-cell aplasia, pure	MESH:D012010	marker/mechanism	6702890
C0034902	hydroxyurea	D006918	127-07-1	red-cell aplasia, pure	MESH:D012010	marker/mechanism	10762306
C0034902	phenytoin	D010672	57-41-0	red-cell aplasia, pure	MESH:D012010	marker/mechanism	146391
C0034902	ticlopidine	D013988	55142-85-3	red-cell aplasia, pure	MESH:D012010	marker/mechanism	18367863
C0034902	tretinoin	D014212	302-79-4	red-cell aplasia, pure	MESH:D012010	marker/mechanism	10609785
C0034902	valproic acid	D014635	99-66-1	red-cell aplasia, pure	MESH:D012010	marker/mechanism	6796707
C0034902	zidovudine	D015215	30516-87-1	red-cell aplasia, pure	MESH:D012010	marker/mechanism	2496734

FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)

FDA labeling changes(Total Drugs:0)
(Waiting for update.)

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