Developmental and speech delay, postnatal microcephaly, and dysmorphic features

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
developmental and speech delay, postnatal microcephaly, and dysmorphic features
MONDO_0060596
BPTF Unknown
28942966 30633344 33522091 36153657
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Developmental and speech delay, postnatal microcephaly, and dysmorphic features.
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Intellectual disability facial dysmorphism skeletal anomalies syndrome 1 shared geneBPTF Related via 1 shared gene including BPTF. Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies 1 shared geneBPTF Related via 1 shared gene including BPTF. 17q24.2 microdeletion syndrome 1 shared geneBPTF Related via 1 shared gene including BPTF. Syndromic intellectual disability 1 shared geneBPTF Related via 1 shared gene including BPTF. Endometrial neoplasms 1 shared geneBPTF Related via 1 shared gene including BPTF.