Results: Enchondromatosis

Results from Abstracts

Pick one of the followings

*Some genes may be words of complete meaning. In any case, if present, they are relevant key words.

Legend:

***	p-value <= 0.001
**	p-value <= 0.01
*	p-value <= 0.05
n.s.	not significant

Top Ranked Genes, Molecules or Short Names*

Blm *
Wrn *
Idh2 n.s.
Recql4 n.s.
Rb1 n.s.
Son n.s.
Col2a1 n.s.
She n.s.
Idh1 n.s.
Ihh n.s.
Mri n.s.
Ptpn11 n.s.
Palm n.s.
Trio n.s.
Ext2 n.s.
Ext1 n.s.
Grasp n.s.
Fgfr3 n.s.
Fh n.s.
Sdhd n.s.
Sdha n.s.
Sdhc n.s.
Gli2 n.s.
Smo n.s.
Pth n.s.
Pthlh n.s.
Pth1r n.s.
Stk11 n.s.
Cltc n.s.
Alk n.s.
Atrx n.s.
Cs n.s.
D2hgdh n.s.
Sdhb n.s.
Rest n.s.
Cast n.s.
Nf1 n.s.
Apc n.s.
Bcr n.s.
Large n.s.
Tp53 n.s.
Met n.s.
Impact n.s.

Top Ranked Mesh Terms

Adult ***
Diagnostic imaging ***
Adolescent ***
Osteochondrodysplasias ***
Female ***
Humans ***
Male ***
Child ***
Chondrosarcoma ***
Radiography ***
Enchondromatosis ***
Diagnosis ***
Pathology ***
Bone neoplasms ***
Child preschool **
Genetics **
Follow-up studies **
Diagnosis differential **
Hemangioma **
Middle aged **
Magnetic resonance imaging **
Chondroma **
Tomography x-ray computed **
Hand **
Brain neoplasms *
Mutation *
Retrospective studies *
Exostoses multiple hereditary *
Dna mutational analysis *
Cell transformation neoplastic *
Metacarpal bones *
Brain stem *
Spinal diseases *
Congenital abnormalities *
Treatment outcome *
History 18th century *
History 17th century *
Museums *
Lumbar vertebrae *
Bone development *
Adipose tissue *
Protein tyrosine phosphatase non-receptor type 11 *
Lymphangioma *
Combined modality therapy *
Achondroplasia *
Hypertrophy *
Genes recessive *
Osteochondroma *
Spine *
Netherlands *
Genes dominant *
Hip joint *
Receptors parathyroid hormone *
Chromosome aberrations *
Neoplasm metastasis *
Peptide hormones *
Frontal lobe *
Hyaline cartilage *
Collagen type ii *
Gene deletion *
Consanguinity *
Neoplastic syndromes hereditary *
Receptor parathyroid hormone type 1 *
Adenoma *
Arm *
Cos cells *
Orthopedic procedures *
Nose neoplasms *
Disease susceptibility *
Rare diseases *
Point mutation *
Skull base neoplasms *
Mosaicism *
Aged 80 and over *
Pons *
Temporal lobe *
Ilium *
Chromosome deletion *
Brain diseases metabolic inborn *
Chromosomes human pair 1 *
Neoplasm recurrence local *
Humerus *
Thoracic vertebrae *
Multimodal imaging *
Parotid neoplasms *
Cell differentiation *
Ulna *
Foot *
Bone and bones *
In situ hybridization fluorescence *
Glutarates *
Klippel-trenaunay-weber syndrome *
Fingers *
Growth plate *
Angiomatosis *
Spinal neoplasms *
Disease progression *
Reoperation *
Bone lengthening *
Biopsy *

Results for: Enchondromatosis

Results from Abstracts

KEGG Pathways

Gene Ontology Biological Processes