Opitz gbbb syndrome, type ii

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Subtype of: Opitz gbbb syndrome
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Opitz GBBB syndrome, type II
MONDO_0017138
SPECC1L Unknown
1897571 21703590 25412741 26111080 8849002
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Opitz gbbb syndrome, type ii.
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Facial clefting, oblique, 1 1 shared geneSPECC1L Related via 1 shared gene including SPECC1L. Opitz gbbb syndrome 1 shared geneSPECC1L Related via 1 shared gene including SPECC1L. Teebi syndrome 1 shared geneSPECC1L Related via 1 shared gene including SPECC1L. Tessier facial cleft 1 shared geneSPECC1L Related via 1 shared gene including SPECC1L. Commissural facial cleft 1 shared geneSPECC1L Related via 1 shared gene including SPECC1L.