P5166
P780
Ollier diseaseThe aggrecanopathies; an evolving phenotypic spectrum of human genetic skeletal diseasesHuman genetic disorders and knockout mice deficient in glycosaminoglycanMaffucci syndrome and neoplasms: a case report and review of the literatureEndoplasmic reticulum stress in chondrodysplasias caused by mutations in collagen types II and XMicrocephalic Osteodysplastic Primordial Dwarfism, Type II: a Clinical ReviewWolcott-Rallison syndromeFrequency and spectrum of Wolcott-Rallison syndrome in Saudi Arabia: a systematic review.Chondrosarcoma of the nasal cavity in a patient with Maffucci syndrome: case report and review of the literature.Tracheobronchopathia osteochondroplastica associated with skin cancer: a case report and review of the literature.Human skeletal dysplasia caused by a constitutive activated transient receptor potential vanilloid 4 (TRPV4) cation channel mutation.[Madelung's deformity: a case report and review of the literature]Tracheobronchopathia Osteochondroplastica: Two Cases Reports and Review of Literature.Stüve-Wiedemann syndrome: LIFR and associated cytokines in clinical course and etiology.A review of the principles of radiological assessment of skeletal dysplasias.Mutations in Biosynthetic Enzymes for the Protein Linker Region of Chondroitin/Dermatan/Heparan Sulfate Cause Skeletal and Skin DysplasiasSclerosing angiomatoid nodular transformation of the spleen in a patient with Maffucci syndrome: a case report and review of literature.
P921
description
Human disease
@en
مرض يصيب الإنسان
@ar
name
Enchondromatosis
@en
enchondromatose
@fr
enkondromatosi
@eu
ورام غضروفي باطن
@ar
type
label
Enchondromatosis
@en
enchondromatose
@fr
enkondromatosi
@eu
ورام غضروفي باطن
@ar
altLabel
Dyschondroplasia (disorder)
@en
Dyschondroplasia NOS (disorder)
@en
Dyschondroplasia
@en
Enchondromatosis (disorder)
@en
Ollier disease
@en
Ollier's disease
@en
dyschondroplasia
@en
enchondromatosis
@en
ورام غضروفي داخلي
@ar
prefLabel
Enchondromatosis
@en
enchondromatose
@fr
enkondromatosi
@eu
ورام غضروفي باطن
@ar
P486
P5806
P6366
P1417
science/enchondromatosis
P1748
P1995
P2888
P31
P3827
enchondromatosis
P486
P492
P5806
P6366
2781395839
P672
C05.116.099.708.338
P673
P699
P7464
ollier-disease