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Details
Link-It Detail - Disease - Osteoarthropathy, Primary Hypertrophic
Debug Stats
  • ### Total Build Time: 194 ms 21.165 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 374 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 616 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
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  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 981 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.764 KB
  • CONCEPT_RELATIONSHIPS gt=168 ms Completed: 168 ms rowSize= 13.554 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 1.532 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Osteoarthropathy, Primary Hypertrophic C0029411
Definition (1)
A conditioned chiefly characterized by thickening of the skin of the head and distal extremities, deep folds and furrows of the skin of the forehead, cheeks, and scalp, seborrhea, hyperhidrosis, periostosis of the long bones, digital clubbing, and spadelike enlargement of the hands and feet. It is more prevalent in the male, and is usually first evident during adolescence. It is believed to be inherited as an autosomal dominant trait. (From Dorland, 27th ed)
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Bone Diseases C0005940
img Joint Diseases C0022408
Ancestral Roots
RootRoot Plus OneDepthParent
img Musculoskeletal Diseases C0026857img Bone Diseases C00059403img Bone Diseases C0005940
img Musculoskeletal Diseases C0026857img Joint Diseases C00224083img Joint Diseases C0022408
Relationships (61)

Relation Types:
diso_​to_​anat : 1
diso_​to_​chem : 2
diso_​to_​diso : 54
diso_​to_​phen : 2
diso_​to_​phys : 2


Relationships:
none : 11
clinically_​similar : 1
manifestation_​of : 44
mapped_​to : 1
mth_​has_​plain_​text_​form : 1
related_​to : 3
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO24img Complication Aspects C1171258
DISO_to_DISO16img Complication Aspects C1171258
DISO_to_PHEN13img genetic aspects C0017399
DISO_to_PHEN8img genetic aspects C0017399
DISO_to_DISO7img Primary Myelofibrosis C0001815
DISO_to_CHEM6img Dehydrogenase, Hydroxyprostaglandin C0020390
DISO_to_CHEM6img Hydroxyprostaglandin Dehydrogenases C0020390
DISO_to_DISO6img Nail Diseases C0027339
DISO_to_DISO5img Arthritis, Psoriatic C0003872
DISO_to_DISO5img Osteoarthropathy, Secondary Hypertrophic C0029412
DISO_to_PHYS5img Mutation C0026882
DISO_to_ANATmanifestation_ofimg Structure of wormian bone C0222716
DISO_to_DISOmanifestation_ofimg Acro-Osteolysis C0917990
DISO_to_DISOmanifestation_ofimg Arthralgia C0003862
DISO_to_DISOmanifestation_ofimg Arthritis C0003864
DISO_to_DISOmanifestation_ofimg BONE LOSS C0029453
DISO_to_DISOmanifestation_ofimg Blepharoptosis C0005745
DISO_to_DISOmanifestation_ofimg Byzanthine arch palate C0240635
DISO_to_DISOrelated_toimg CIO C2678441
DISO_to_DISOrelated_toimg CRANIOOSTEOARTHROPATHY C2678439
DISO_to_DISOmanifestation_ofimg Caused by mutation in the 15-alpha-hydroxyprostaglandin dehydrogenase gene (HPGD, 601688.0001). C2749460
DISO_to_DISOmanifestation_ofimg Clubbed Fingers C0009080
DISO_to_DISOmanifestation_ofimg Coarse facial features C1854600
DISO_to_DISOmanifestation_ofimg Congenital funnel chest C0016842
DISO_to_DISOmanifestation_ofimg Decreased joint mobility C1857108
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanHPGD3248hydroxyprostaglandin dehydrogenase 15-(NAD)
img GENERIF, Score=1000, Pubmed Id: 18500342, UMLKSK CUI: C0029411
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0029411Osteoarthropathy, Primary Hypertrophic0self