Medical Subject Headings

Last uploaded: August 28, 2024
Preferred Name

Hyperostosis, Cortical, Congenital
Synonyms

Disease, Familial Caffey's

Hyperostosis, Infantile Cortical

Cortical Congenital Hyperostoses

Cortical Hyperostosis, Infantile

Familial Caffeys Disease

Infantile Cortical Hyperostoses

Congenital Cortical Hyperostoses

Caffey De Toni Silvermann Syndrome

Cortical Hyperostoses, Infantile

Congenital Hyperostoses, Cortical

Familial Caffey Disease

Syndrome, Caffey-De Toni-Silvermann

Disease, Caffey

Familial Infantile Cortical Hyperostosis

Hyperostoses, Cortical Congenital

Hyperostosis, Cortical Congenital

Hyperostoses, Congenital Cortical

Cortical Congenital Hyperostosis

Infantile Cortical Hyperostosis

Congenital Cortical Hyperostosis

Familial Caffey's Disease

Caffey's Disease, Familial

Hyperostosis, Congenital Cortical

Hyperostoses, Infantile Cortical

Caffey Disease

Congenital Hyperostosis, Cortical

Cortical Hyperostoses, Congenital

Cortical Hyperostosis, Congenital

Caffey-De Toni-Silvermann Syndrome

Definitions

A disease of young infants characterized by soft tissue swellings over the affected bones, fever, and irritability, and marked by periods of remission and exacerbation. (Dorland, 27th ed)

ID

http://purl.bioontology.org/ontology/MESH/D006958

altLabel

Disease, Familial Caffey's

Hyperostosis, Infantile Cortical

Cortical Congenital Hyperostoses

Cortical Hyperostosis, Infantile

Familial Caffeys Disease

Infantile Cortical Hyperostoses

Congenital Cortical Hyperostoses

Caffey De Toni Silvermann Syndrome

Cortical Hyperostoses, Infantile

Congenital Hyperostoses, Cortical

Familial Caffey Disease

Syndrome, Caffey-De Toni-Silvermann

Disease, Caffey

Familial Infantile Cortical Hyperostosis

Hyperostoses, Cortical Congenital

Hyperostosis, Cortical Congenital

Hyperostoses, Congenital Cortical

Cortical Congenital Hyperostosis

Infantile Cortical Hyperostosis

Congenital Cortical Hyperostosis

Familial Caffey's Disease

Caffey's Disease, Familial

Hyperostosis, Congenital Cortical

Hyperostoses, Infantile Cortical

Caffey Disease

Congenital Hyperostosis, Cortical

Cortical Hyperostoses, Congenital

Cortical Hyperostosis, Congenital

Caffey-De Toni-Silvermann Syndrome

AN

cortical refers to cortex of bone; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES

AQL

BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI

cui

C0020497

DC

1

definition

A disease of young infants characterized by soft tissue swellings over the affected bones, fever, and irritability, and marked by periods of remission and exacerbation. (Dorland, 27th ed)

DX

19640101

HN

91; was HYPEROSTOSIS, CORTICAL CONGENITAL 1964-90

Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000469

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000401

Machine permutation

91; was HYPEROSTOSIS, CORTICAL CONGENITAL 1964-90

Mapped from

http://purl.bioontology.org/ontology/MESH/C566473

http://purl.bioontology.org/ontology/MESH/C566870

http://purl.bioontology.org/ontology/MESH/C537021

http://purl.bioontology.org/ontology/MESH/C537020

http://purl.bioontology.org/ontology/MESH/C536748

http://purl.bioontology.org/ontology/MESH/C566184

MDA

19990101

MMR

20120703

MN

C05.116.099.708.479

C16.614.465

C05.116.540.400

notation

D006958

OL

use HYPEROSTOSIS, CORTICAL, CONGENITAL to search HYPEROSTOSIS, CORTICAL CONGENITAL 1966-90

prefLabel

Hyperostosis, Cortical, Congenital

TERMUI

T781891

T781889

T020901

T781890

T020902

T020899

T020900

T020903

T020904

TH

OMIM (2013)

NLM (1991)

NLM (2012)

UNK (19XX)

NLM (1964)

ORD (2010)

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D010009

http://purl.bioontology.org/ontology/MESH/D007232

http://purl.bioontology.org/ontology/MESH/D015576

Delete Subject Author Type Created
No notes to display
Create mapping