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Details
Link-It Detail - Disease - Abnormal development of cartilage
Debug Stats
  • ### Total Build Time: 92 ms 16.515 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 364 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 222 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=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=75 ms Completed: 75 ms rowSize= 13.337 KB
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 1.368 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Abnormal development of cartilage C0008449
Definition (1)
morbid condition characterized by abnormal development of cartilage.
Relationships (56)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 54


Relationships:
classifies : 2
expanded_​form_​of : 1
is_​normal_​tissue_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 15
mapped_​to : 35
use : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATis_normal_tissue_origin_of_diseaseimg Connective and Soft Tissue C1516798
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Skeletal bone C0262950
DISO_to_DISOmapped_toimg ACG2 C0220685
DISO_to_DISOmapped_toimg AOI C0265283
DISO_to_DISOexpanded_form_ofimg Abnormal development of cartilage C0008449
DISO_to_DISOmapped_toimg Achondrogenesis C0001079
DISO_to_DISOmapped_toimg Achondrogenesis, type IB (disorder) C0265274
DISO_to_DISOmapped_toimg Achondroplasia C0001080
DISO_to_DISOisaimg Agenesis of nasal cartilages C0339851
DISO_to_DISOclassifiesimg All other congenital anomalies C0810365
DISO_to_DISOisaimg Anomaly of cricoid cartilage C0265751
DISO_to_DISOisaimg Anomaly of thyroid cartilage C0265753
DISO_to_DISOisaimg Anomaly of tracheal cartilage C0265773
DISO_to_DISOmapped_toimg Biochemical rickets C0458011
DISO_to_DISOmapped_toimg CHH C0220748
DISO_to_DISOmapped_toimg CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE C1300226
DISO_to_DISOisaimg CHONDRODYSTROPHY, HYPOPLASTIC C0520553
DISO_to_DISOmapped_toimg Cartilage hair syndrome with associated immunodeficiency C0582477
DISO_to_DISOmapped_toimg Chondrodysplasia C0343284
DISO_to_DISOmapped_toimg Chondrodysplasia OS C0432229
DISO_to_DISOmapped_toimg Chondrodysplasia with Hemangioma C0024454
DISO_to_DISOisaimg Chondrodystrophy malacia C0520554
DISO_to_DISOisaimg Congenital anomaly of rib cartilage C0685634
DISO_to_DISOisaimg Congenital bronchomalacia C0340242
DISO_to_DISOisaimg Congenital cartilage anomaly of third eyelid C0521581
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanLBR3930lamin B receptor
img OMIM, Score=790, UMLKSK CUI: C0008449
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0008449Abnormal development of cartilage0self