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Details
Link-It Detail - Human Phenotype - Abnormality of the meninges
Debug Stats
  • ### Total Build Time: 225 ms 26.180 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 202 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 324 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
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 820 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.983 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.133 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=218 ms Completed: 218 ms rowSize= 18.583 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the meninges HP:0010651
Definition (1)
An abnormality of the `Meninges` (FMA:231572), including any abnormality of the `Dura mater` (FMA:9592), the `Arachnoid mater` (FMA:9591), and the `Pia mater` (FMA:9590).
Parents (2)
img Abnormality of the central nervous system HP:0002011
img Morphological abnormality of the central nervous system HP:0007319
Children (9)
img Meningitis HP:0001287
img Meningocele HP:0002435
img Meningeal calcification HP:0100250
img Ivory epiphyses HP:0010583
img Abnormality of the pia mater HP:0100701
img Abnormality of the dura mater HP:0010652
img Abnormality of the spinal meninges HP:0010303
img Abnormality of the arachnoid mater HP:0100700
img Epiphyseal stippling HP:0010655
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the central nervous system HP:0002011
img All HP:0000001img Phenotypic abnormality HP:00001186img Morphological abnormality of the central nervous system HP:0007319
Genes (103)

Species:
human : 103
Page Size
Current 25
  Page 1 of 5
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanFL1100306940Follicular lymphoma, susceptibility to, 1
img HP RolledUp, OMIM ID: 613024
HumanIH100188864Hemihypertrophy
HumanWG474168Wegener granulomatosis
img HP RolledUp, OMIM ID: 608710
HumanFREM2341640FRAS1 related extracellular matrix protein 2
HumanSUMF1285362sulfatase modifying factor 1
img HP RolledUp, OMIM ID: 272200
HumanWDR62284403WD repeat domain 62
img HP RolledUp, OMIM ID: 600176
HumanADAMTS18170692ADAM metallopeptidase with thrombospondin type 1 motif, 18
HumanBMPER168667BMP binding endothelial regulator
img HP RolledUp, OMIM ID: 608022
HumanTNFRSF13C115650tumor necrosis factor receptor superfamily, member 13C
img HP RolledUp, OMIM ID: 240500
HumanNLRP3114548NLR family, pyrin domain containing 3
img HP RolledUp, OMIM ID: 607115
HumanCEP4195681centrosomal protein 41kDa
HumanTMEM6791147transmembrane protein 67
img HP RolledUp, OMIM ID: 607361
HumanSHANK385358SH3 and multiple ankyrin repeat domains 3
img HP RolledUp, OMIM ID: 606232
HumanVANGL181839VANGL planar cell polarity protein 1
img HP RolledUp, OMIM ID: 600145
HumanITPKC80271inositol-trisphosphate 3-kinase C
img HP RolledUp, OMIM ID: 611775
HumanFUZ80199fuzzy planar cell polarity protein
HumanFRAS180144Fraser syndrome 1
HumanTCTN279867tectonic family member 2
HumanTTC21B79809tetratricopeptide repeat domain 21B
HumanTMEM23179583transmembrane protein 231
HumanC5orf4265250chromosome 5 open reading frame 42
HumanCARD964170caspase recruitment domain family, member 9
img HP RolledUp, OMIM ID: 212050
HumanXPNPEP363929X-prolyl aminopeptidase (aminopeptidase P) 3, putative
img HP RolledUp, OMIM ID: 613159
HumanRFMN57788Roifman syndrome
img HP RolledUp, OMIM ID: 300258
HumanINPP5E56623inositol polyphosphate-5-phosphatase, 72 kDa
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010651Abnormality of the meninges0self