transverse myelitis

A myelitis that is characterized by a band-like sensation across the trunk of the body, with sensory changes below.

patent blue V allergy

A drug allergy that has_allergic_trigger patent blue V.

Lisch epithelial corneal dystrophy

An epithelial and subepithelial dystrophy that is characterized by bilateral or unilateral, gray, band-shaped, and feathery opacities that sometimes appeared in whorled patterns and that has_material_basis_in the MCOLN1 gene on Chr. 19.

mitochondrial complex V (ATP synthase) deficiency nuclear type 1

A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in mutation in the ATPAF2 gene on chromosome 17p11.

mitochondrial complex V (ATP synthase) deficiency nuclear type 3

A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in mutation in the ATP5E gene on chromosome 20q13.

mitochondrial complex V (ATP synthase) deficiency nuclear type 2

A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in mutation in the TMEM70 gene on chromosome 8q21.

mitochondrial complex V (ATP synthase) deficiency nuclear type 4

A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in mutation in the ATP5F1A gene on chromosome 18q21.1.

mitochondrial complex V (ATP synthase) deficiency nuclear type 5

A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in homozygous mutation in the ATP5F1D gene on chromosome 19p13.3.

subcortical band heterotopia

A congenital nervous system abnormality characterized by migration of neurons to ectopic locations in the brain where the neurons form areas that appear as band-like clusters of white tissue underneath the gray tissue of the cerebral cortex.

lissencephaly 5

A lissencephaly characterized by hydrocephalus, seizures, severely delayed psychomotor development, and cobblestone changes in the cortex, more severe in the posterior region, and subcortical band heterotopia that has_material_basis_in homozygous or compound heterozygous mutation in the LAMB1 gene on chromosome 7q31.1.