Male with structurally abnormal sex chromosome
Q93.89 Other deletions from the autosomes Notes: Deletions identified by fluorescence in situ hybridization (FISH) ; Deletions …
Other deletions from the autosomes Notes: Deletions identified by fluorescence in situ hybridization (FISH) ; Deletions identified by in situ hybridization (ISH) ; Deletions seen only at prometaphase
Q96.8 Other variants of Turner’s syndrome
Other variants of Turner's syndrome
Q98.7 Male with sex chromosome mosaicism
Male with sex chromosome mosaicism
Q76.428 Congenital lordosis, sacral and sacrococcygeal region
Congenital lordosis, sacral and sacrococcygeal region
Q77.7 Spondyloepiphyseal dysplasia
Spondyloepiphyseal dysplasia
Q79.2 Exomphalos Notes: Omphalocele ; umbilical hernia (K42.-)
Exomphalos Notes: Omphalocele ; umbilical hernia (K42.-)
Q80.1 X-linked ichthyosis
X-linked ichthyosis