Disease Index

human disease

carcinoma (i.e. not a sarcoma) showing clear cells

medical condition

human disease

human disease

Cleft lip and alveolus is a fissure type embryopathy that involves the upper lip, nasal base and alveolar ridge in variable degrees

congenital malformations caused by the failure of embryonic structures of the lip and/or palate to fuse

human disease

Human disease

Cleft lip - retinopathy is an exceedingly rare association characterized by cleft lip and progressive retinopathy

human disease

human disease

orofacial cleft characterized by a fissure of the soft and/or hard palate, due to faulty fusion of the two plates of the skull that form the hard palate

physical disorder that is characterized by fusion of maxilla and mandible with autosomal dominant inheritance

medical condition

Cleft velum is a fissure type embryopathy that affects in varying degrees the soft palate

osteochondrodysplasia that has material basis in mutations in the RUNX2 gene which results in undeveloped or absent located in clavicle along with delayed closing of fontanels in the located in skull

human disease

bladder exstrophy-epispadias-cloacal exstrophy complex that is characterized by a defect in the urethra, bladder and bowel

human disease

human disease

Human disease

human disease

This newly described syndrome is characterized by cloverleaf skull, limb anomalies, facial dysmorphism and multiple congenital anomalies

CLOVE syndrome is characterized by Congenital Lipomatous Overgrowth, progressive, complex and mixed truncal Vascular malformations, and Epidermal nevi

genetic trait