3-M syndrome and CCDC8

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between 3-M syndrome and CCDC8

3-M syndrome vs. CCDC8

3-M syndrome is a rare hereditary disorder characterized by severe growth retardation, facial dysmorphia, and skeletal abnormalities. Coiled-coil domain containing 8 is a protein that in humans is encoded by the CCDC8 gene.

Similarities between 3-M syndrome and CCDC8

3-M syndrome and CCDC8 have 1 thing in common (in Unionpedia): OBSL1.

OBSL1

Obscurin-like protein 1 is a protein that in humans is encoded by the OBSL1 gene.

3-M syndrome and OBSL1 · CCDC8 and OBSL1 · See more »

The list above answers the following questions

What 3-M syndrome and CCDC8 have in common
What are the similarities between 3-M syndrome and CCDC8

3-M syndrome and CCDC8 Comparison

3-M syndrome has 26 relations, while CCDC8 has 7. As they have in common 1, the Jaccard index is 3.03% = 1 / (26 + 7).

References

This article shows the relationship between 3-M syndrome and CCDC8. To access each article from which the information was extracted, please visit:

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