Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin

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Subtype of: Macrocephaly
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin
MONDO_0859231
ZBTB7A Causal
34515416 31645653
Open Targets —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin.
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Intellectual developmental disorder dysmorphic macrocephaly 1 shared geneZBTB7A Related via 1 shared gene including ZBTB7A. Developmental disorder with macrocephaly, obstructive sleep apnea, and persistent fetal hemoglobin 1 shared geneZBTB7A Related via 1 shared gene including ZBTB7A. Upper respiratory tract disorder 1 shared geneZBTB7A Related via 1 shared gene including ZBTB7A. Erythematosquamous dermatosis 1 shared geneZBTB7A Related via 1 shared gene including ZBTB7A. Pharyngeal disorder 1 shared geneZBTB7A Related via 1 shared gene including ZBTB7A.