ZC4H2 deficiency
ZC4H2 (Zinc finger C4H2-type) is a protein-coding gene located on the X-chromosome. This gene encodes a protein which is a member of the so-called zinc finger domain-containing protein family. There is currently very limited understanding about the ZC4H2 gene and its protein function. Any pathogenic variant of ZC4H2 which is associated with a clinical phenotype is referred to as "ZC4H2 Deficiency".
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ZC4H2 deficiency
ZC4H2 (Zinc finger C4H2-type) is a protein-coding gene located on the X-chromosome. This gene encodes a protein which is a member of the so-called zinc finger domain-containing protein family. There is currently very limited understanding about the ZC4H2 gene and its protein function. Any pathogenic variant of ZC4H2 which is associated with a clinical phenotype is referred to as "ZC4H2 Deficiency".
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ZC4H2 (Zinc finger C4H2-type) ...... an ultra-rare orphan disorder.
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ZC4H2 (Zinc finger C4H2-type) ...... rred to as "ZC4H2 Deficiency".
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ZC4H2 deficiency
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