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Details
Link-It Detail - Human Phenotype - Abnormality of erythroid lineage cell
Debug Stats
  • ### Total Build Time: 35 ms 22.649 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 212 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 212 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_NAMESPACE gt=0 Completed: 0 ms rowSize= 168 bytes
  • CONCEPT_PARENTS gt=10 ms Completed: 10 ms rowSize= 468 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 450 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.183 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 18.816 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.031 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of erythroid lineage cell HP:0010973
Definition (1)
An abnormality of a `erythroid lineage cell` (CL:0000764).
Namespace (1)
medical_genetics
Parents (1)
img Abnormality of blood and blood-forming tissues HP:0001871
Children (1)
img Abnormality of erythrocytes HP:0001877
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of blood and blood-forming tissues HP:0001871
Genes (324)

Species:
human : 324
Page Size
Current 25
  Page 1 of 13
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
HumanAMMEC100499260Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis
img HP RolledUp, OMIM ID: 300194
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
HumanTEC100124696transient erythroblastopenia of childhood
HumanKTWS791122Klippel-Trenaunay-Weber syndrome
img HP RolledUp, OMIM ID: 149000
HumanMPDMRS574047Martin-Probst deafness-mental retardation syndrome
img HP RolledUp, OMIM ID: 300519
HumanCOA5493753cytochrome c oxidase assembly factor 5
HumanSLEB4404714systemic lupus erythematosus, susceptibility to, 4
HumanLCRB387281locus control region, beta
img HP RolledUp, OMIM ID: 141749
img HP RolledUp, OMIM ID: 604131
img HP RolledUp, OMIM ID: 613985
HumanMMAB326625methylmalonic aciduria (cobalamin deficiency) cblB type
HumanRAB40AL282808RAB40A, member RAS oncogene family-like
img HP RolledUp, OMIM ID: 300519
HumanNPHP4261734nephronophthisis 4
HumanUNC13D201294unc-13 homolog D (C. elegans)
img HP RolledUp, OMIM ID: 608898
HumanFLCN201163folliculin
HumanNLRP7199713NLR family, pyrin domain containing 7
img HP RolledUp, OMIM ID: 231090
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanRLS192142Restless legs syndrome, susceptibility to
HumanSLEH1170682systemic lupus erythematosus with hemolytic anemia 1
HumanMMAA166785methylmalonic aciduria (cobalamin deficiency) cblA type
HumanTMPRSS6164656transmembrane protease, serine 6
HumanCDAN1146059codanin 1
HumanDNAJC19131118DnaJ (Hsp40) homolog, subfamily C, member 19
HumanCYP4F22126410cytochrome P450, family 4, subfamily F, polypeptide 22
img HP RolledUp, OMIM ID: 604777
HumanNLRP3114548NLR family, pyrin domain containing 3
img HP RolledUp, OMIM ID: 191900
img HP RolledUp, OMIM ID: 607115
HumanDBA2114086Diamond-Blackfan anemia 2
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010973Abnormality of erythroid lineage cell0self