Disease Index

Methemoglobinemia that is caused by exposure to certain drugs (xylocaine and benzene)

skin hypersensitivity reaction due to exposure to a pharmacologic substance that is characterized by raised purpuric lesions, red macules, hemorrhagic blisters and ulcerations

human disease

potential harm or negative consequences to the fetus due to drugs and medications during pregnancy

bone malformation affecting arms and legs

a rare congenital disease characterized by external gaze palsy

autosomal dominant disease characterized by upper limb anomalies, ocular anomalies, and, in some cases, renal anomalies and that has material basis in heterozygous mutation in the SALL4 gene on chromosome 20q13

rare, autosomal recessive, benign disorder that causes an isolated increase of conjugated bilirubin in the serum

genetic disorder

Duchenne and Becker muscular dystrophies (DMD and BMD) are neuromuscular diseases characterized by progressive muscle wasting and weakness due to degeneration of skeletal, smooth and cardiac muscle

neuromuscular disease characterized by rapidly progressive muscle weakness and wasting due to degeneration of skeletal, smooth and cardiac muscle

Duchenne muscular dystrophy (DMD) is a severe type of muscular dystrophy that primarily affects boys.

medical condition

congenital disorder of digestive system

well differentiated, low or intermediate grade tumor with neuroendocrine differentiation that arises from the duodenum

human disease

human disease

human disease

rare genetic disease

human disease

human disease

rare skeletal disorder belonging to the group of spondyloepimetaphyseal dysplasias

human disease

Dyschondrosteosis - nephritis is characterized by the association of short stature due to mesomelic shortening of the limbs and Madelung deformity (see this term), with hereditary nephritis

pigmentation disease characterized by progressively pigmented and depigmented macules, often mixed in a reticulate pattern, concentrated on the dorsal extremities

pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution

human disease

type of brain tumour

Dysequilibrium syndrome (DES) is a non-progressive cerebellar disorder characterized by ataxia associated with an intellectual disability, delayed ambulation and cerebellar hypoplasia