223800.G.2

Country

Morocco

HPO Terms

Postnatal growth retardation; Microcephaly; Abnormal facial shape; Abnormal thorax morphology; Scoliosis; Rhizomelia; Intellectual disability; Platyspondyly; Epiphyseal dysplasia; Metaphyseal dysplasia; Iliac crest serration

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Sex

Unknown

Parental Consanguinity

Yes

Subject Variants

Variant Name	Allele Count	Allele Frequency	Associated Disease	Associated Gene
NM_017653.6:c.1878del	6	NA	Dyggve-Melchior-Clausen Disease

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Remarks

3 patients from Family 3 in the publication

References

El Ghouzzi et al. 2003