Human genes for chromosome 15q26-qter deletion syndrome
Chromosome 15q26-qter deletion syndrome [DOID:0060397]
A chromosomal deletion syndrome that is characterized by pre- and postnatal growth restriction, developmental delay, variable degrees of intellectual disability, brachy-clinodactyly, talipes equinovarus, nail hypoplasia, proximally placed digits and mild craniofacial dysmorphism including microcephaly, triangular face, broad nasal bridge and micrognathia.
Synonyms: chromosome 15q26-qter deletion syndrome, chromosome 15q26qter deletion syndrome, chromosome 15q26-qter deletion disease, chromosome 15q26-qter deletion disorder, DOID:0060397 ...