Disease Index

medical condition

human disease

skin disease in which dry, scaly skin accumulates

non-hereditary form of ichthyosis characterized by plate-like scales on the legs, arms and occasionally the torso

human disease

ia rare keratinopathic ichthyosis characterized by the presence of superficial blisters and erosions at birth

human disease

Ichthyosis follicularis - alopecia - photophobia (IFAP) is a rare genetic disorder characterized by the triad of ichthyosis follicularis, alopecia, and photophobia from birth

group of rare skin disorders in the ichthyosis family of skin

medical condition

skin disorder

human disease

Ichthyosis-cheek-eyebrow syndrome is characterised by ichthyosis, prominent full cheeks and sparse lateral eyebrows. It has been described in several individuals from four generations of one family. Transmission is autosomal dominant.

Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome is characterised by ichthyosis, hepatosplenomegaly and late-onset cerebellar ataxia. It has been described in two brothers. Transmission is either autosomal recessive or X-linked.

genetic disorder

Idiopathic achalasia (IA) is a primary esophageal motor disorder characterized by loss of esophageal peristalsis and insufficient lower esophageal sphincter (LES) relaxation in response to deglutition

Idiopathic acute transverse myelitis (ATM) is an immune-mediated inflammatory demyelinating disorder of the spinal cord with motor, sensory and autonomic involvement

human disease

human disease

human disease

human disease

human disease