Disease Index

human disease

ovarian carcinoma that derives from epithelial cells of glandular origin

genetic disease

This syndrome is characterised by tall stature, learning difficulties and facial dysmorphism

human disease

human disease

Overlap myositis (OM) is a form of idiopathic inflammatory myopathy (IIM) characterized by myositis with at least one clinical and/or autoantibody overlap feature

sexual ambiguity in which the individual possesses tissues from the ovary and the testis

Human disease

cephalic disorder where the top of the skull is pointed or conical due to premature closure of the coronal suture plus any other suture

rare group of autosomal dominant skin disorders that are caused by a mutation in one of five different keratin genes

medical condition

bone formation disease that has material basis in hyperactive osteoclast which results in abnormal osteoblast bone formation located in skull, located in pelvis, located in vertebral column, located in set of limbs

medical condition

PAGOD syndrome is a severe developmental syndrome characterized by multiple congenital anomalies including cardiovascular defects, pulmonary hypoplasia, diaphragmatic defects and genital anomalies

Median cleft of the upper lip-corpus callosum lipoma-cutaneous polyps syndrome

human disease

human disease

human disease

Human disease

rare disease

human disease

medical condition

Keratosis, Nagashima-type is a transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda (see this term)

keratosis characterized by abnormal thickening of the palms and the soles

neoplasm (disease) that involves the skin of eyelid

lentigo that involves the skin of eyelid