Craniofacial dysmorphism, hypoplasia of scapula and pelvis, and short stature (cousin syndrome)

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Cousin syndrome
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
craniofacial dysmorphism, hypoplasia of scapula and pelvis, and short stature (Cousin syndrome)
MONDO_0009845
TBX15 Unknown
19068278 24039145
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Craniofacial dysmorphism, hypoplasia of scapula and pelvis, and short stature (cousin syndrome).
5 View disease cluster →
Cousin syndrome 1 shared geneTBX15 Related via 1 shared gene including TBX15. Pelviscapular dysplasia 1 shared geneTBX15 Related via 1 shared gene including TBX15. Chagas cardiomyopathy 1 shared geneTBX15 Related via 1 shared gene including TBX15. Growth disorder 1 shared geneTBX15 Related via 1 shared gene including TBX15. Obstructive sleep apnea syndrome 1 shared geneTBX15 Related via 1 shared gene including TBX15.