Parietal foramina

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
PARIETAL FORAMINA
C1868598MESH:C566826MONDO:0018953
ALX4 Unknown
11137991 16319823
CTD, Disgenet, GWAS catalog —
MSX2 Unknown
10742103 10742104 10767351 11137991 14571277 15198690 16222674 16319823 16642368
CTD, ClinGen, Disgenet, GWAS catalog
PARIETAL FORAMINA 1
168500C1868599MONDO:0008197
MSX2 Causal
10742103 10742104 10767351 14571277 16222674 16319823
ClinVar, Disgenet, HPO
PARIETAL FORAMINA 2
609597C1865044MESH:C566510MONDO:0012309
ALX4 Causal
11106354 23401352 24764194 34315693
CTD, ClinVar, Disgenet, GenCC, HPO —
PARIETAL FORAMINA WITH CLAVICULAR HYPOPLASIA
251290
MSX2 Unknown — Orphanet
PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA
168550C1868597MESH:C566825MONDO:0008198
MSX2 Causal
14571277
CTD, ClinVar, Disgenet, HPO, ClinGen
All2 Causal2 Unknown2
Related Diseases Diseases that share the most curated genes with Parietal foramina.
5 View disease cluster →
craniosynostosis 2 1 shared geneMSX2 Related via 1 shared gene including MSX2. Frontonasal dysplasia with alopecia and genital anomaly 1 shared geneALX4 Related via 1 shared gene including ALX4. 11p11.2 deletion syndrome 1 shared geneALX4 Related via 1 shared gene including ALX4. Potocki-shaffer syndrome 1 shared geneALX4 Related via 1 shared gene including ALX4. Frontonasal dysplasia 1 shared geneALX4 Related via 1 shared gene including ALX4.