MSX2, msh homeobox 2, 4488

N. diseases: 135; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1868598
Disease: PARIETAL FORAMINA
PARIETAL FORAMINA 		0.850 Biomarker disease CTD_human
CUI: C1868598
Disease: PARIETAL FORAMINA
PARIETAL FORAMINA 		0.850 Biomarker disease HPO
CUI: C1868598
Disease: PARIETAL FORAMINA
PARIETAL FORAMINA 		0.850 CausalMutation disease CLINVAR
CUI: C1858160
Disease: CRANIOSYNOSTOSIS, TYPE 2
CRANIOSYNOSTOSIS, TYPE 2 		0.800 CausalMutation disease CLINVAR
CUI: C1858160
Disease: CRANIOSYNOSTOSIS, TYPE 2
CRANIOSYNOSTOSIS, TYPE 2 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C1858160
Disease: CRANIOSYNOSTOSIS, TYPE 2
CRANIOSYNOSTOSIS, TYPE 2 		0.800 Biomarker disease CTD_human
CUI: C1868597
Disease: Parietal Foramina With Cleidocranial Dysplasia
Parietal Foramina With Cleidocranial Dysplasia 		0.710 Biomarker disease GENOMICS_ENGLAND
CUI: C1868597
Disease: Parietal Foramina With Cleidocranial Dysplasia
Parietal Foramina With Cleidocranial Dysplasia 		0.710 GermlineCausalMutation disease ORPHANET
CUI: C1868597
Disease: Parietal Foramina With Cleidocranial Dysplasia
Parietal Foramina With Cleidocranial Dysplasia 		0.710 CausalMutation disease CLINVAR
CUI: C1868597
Disease: Parietal Foramina With Cleidocranial Dysplasia
Parietal Foramina With Cleidocranial Dysplasia 		0.710 Biomarker disease CTD_human
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		0.600 Biomarker disease MGD
CUI: C1868599
Disease: PARIETAL FORAMINA 1
PARIETAL FORAMINA 1 		0.600 CausalMutation disease CLINVAR
CUI: C1868599
Disease: PARIETAL FORAMINA 1
PARIETAL FORAMINA 1 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		0.110 Biomarker disease HPO
CUI: C0018681
Disease: Headache
Headache 		0.110 Biomarker phenotype HPO
CUI: C4023418
Disease: Unicoronal synostosis
Unicoronal synostosis 		0.110 Biomarker disease HPO
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		0.100 Biomarker disease HPO
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		0.100 Biomarker disease HPO
CUI: C0011649
Disease: Dermoid Cyst
Dermoid Cyst 		0.100 Biomarker disease HPO
CUI: C0036572
Disease: Seizures
Seizures 		0.100 Biomarker phenotype HPO
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		0.100 Biomarker disease HPO
CUI: C0221354
Disease: Frontal bossing
Frontal bossing 		0.100 Biomarker disease HPO
CUI: C0221355
Disease: Macrocephaly
Macrocephaly 		0.100 Biomarker disease HPO
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly 		0.100 Biomarker disease HPO
CUI: C0426799
Disease: Congenital hypoplasia of clavicle
Congenital hypoplasia of clavicle 		0.100 Biomarker disease HPO