Congenital pontocerebellar hypoplasia type 12

Parents (11)

• 205402004Arthrogryposis multiplex congenita disorder
• 85995004Autosomal recessive hereditary disorder disorder
• 45163000Congenital pontocerebellar hypoplasia disorder
• 76349003Extrapyramidal disease disorder
• 199531009Fetal hereditary disease disorder
• 431265009Fetal microcephaly disorder
• 363235000Hereditary disorder of nervous system disorder
• 28204005Inherited arthrogryposis disorder
• 65094009Multiple malformation syndrome with facial defects as major feature disorder
• 204081007Spinal cord hypoplasia disorder
• 91502009Spinocerebellar disease disorder

Children (0)

None (leaf concept).