Frontonasal dysplasia

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
FRONTONASAL DYSPLASIA
C1876203MESH:C538065MONDO:0016643
ALX1 Unknown — CTD, Disgenet —
ALX3 Unknown
19409524
CTD, Disgenet —
ALX4 Unknown — CTD, Disgenet —
EFNB1 Unknown
15166289
CTD, Disgenet
IRX5 Unknown
22581230
CTD, Disgenet —
KCTD15 Unknown
38296633
Disgenet, GenCC —
SIX2 Unknown
18570229
CTD, Disgenet —
FRONTONASAL DYSPLASIA 1
136760
ALX3 Unknown
19409524 22106187 29215096 34098755
HPO —
FRONTONASAL DYSPLASIA 2
613451C3150703
ALX4 Unknown
19692347 22140057 24668755 29681084 32216639 39157323
Disgenet, HPO —
FRONTONASAL DYSPLASIA 3
613456C3150706
ALX1 Unknown
20451171 27324866
Disgenet, HPO —
All7 Causal0 Unknown7
Related Diseases Diseases that share the most curated genes with Frontonasal dysplasia.
5 View disease cluster →
Frontonasal dysplasia with alopecia and genital anomaly 1 shared geneALX4 Related via 1 shared gene including ALX4. craniofacial dysplasia - osteopenia syndrome 1 shared geneIRX5 Related via 1 shared gene including IRX5. Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome 1 shared geneALX1 Related via 1 shared gene including ALX1. frontorhiny 1 shared geneALX3 Related via 1 shared gene including ALX3. Parietal foramina 1 shared geneALX4 Related via 1 shared gene including ALX4.