Disease Index

human disease

human disease

rare inflammatory brain disease

human disease

human disease

Human disease

Brachydactyly-nystagmus-cerebellar ataxia syndrome is characterized by brachydactyly, nystagmus and cerebellar ataxia. Intellectual deficit and strabismus are also reported in some patients.

disease

Human disease

medical condition

Bifid uvula is a fissure type embryopathy affecting the uvula at the back of the soft palate

eye disease

medical condition

human disease

This syndrome is characterized by the association of bilateral microtia with severe to profound hearing impairment, and cleft palate

human disease

human disease

renal agenesis that is characterized by the absence of both kidneys at birth

severe damage to both inner ears

Bile acid CoA ligase deficiency and defective amidation is an anomaly of bile acid synthesis (see this term) characterized by fat malabsorption, neonatal cholestasis and growth failure

human disease

congenital disorder of digestive system investigation of choice of the disease is MRCP

human disease

disease involving the biliary tree

acute leukemia of ambiguous lineage in which there is a dual population of blasts with each population expressing markers of a distinct lineage (myeloid and lymphoid or B-and T-lymphocyte). (WHO, 2001) -- 2003

Human disease

human disease

Human disease