Disease Directory

Bardet-Biedl syndrome 18 is a rare genetic disorder that is part of the Bardet-Biedl syndrome group. It is defined by a mutation in the BBIP1 gene, wh...

Bardet-Biedl syndrome 19 is a rare inherited condition that is part of a group of disorders known as Bardet-Biedl syndromes. This specific type is cau...

Bardet-Biedl syndrome 2 is a rare genetic condition that is part of the Bardet-Biedl syndrome group. It is specifically caused by a mutation in the BB...

Bardet-Biedl syndrome 20 (BBS20) is a rare genetic condition noted in clinical databases with the OMIM entry OMIM:619471. Although detailed descriptio...

Bardet-Biedl syndrome 22 is a rare inherited condition that is part of a group of disorders known as Bardet-Biedl syndromes. It is caused by a mutatio...

Bardet-Biedl syndrome 3 is a multisystem condition that affects several organ systems including the eyes, limbs, and neurological development. It is c...

Bardet-Biedl syndrome 4 is a multisystem disorder that affects processes including vision, reproductive development, and cognitive function. The condi...

Bardet-Biedl syndrome 5 is a type of Bardet-Biedl syndrome that is caused by a mutation in the BBS5 gene. This condition is part of a larger group of...

Bardet-Biedl syndrome 6 is a multisystem condition that affects several body systems including the eyes, limbs, metabolic regulation, and cognitive de...

Bardet-Biedl syndrome 7 is a rare genetic condition that is part of the Bardet-Biedl syndrome group. It is caused by a mutation in the BBS7 gene. This...

Bardet-Biedl syndrome 8 is a rare genetic condition that belongs to a group of disorders known as Bardet-Biedl syndromes. This condition is specifical...

Bardet-Biedl syndrome 9 is a rare genetic disorder that is part of the Bardet-Biedl syndrome group. This condition is caused by a mutation in the BBS9...

Barrett adenocarcinoma is a type of cancer that starts in the cells of the esophagus. It arises from Barrett metaplastic epithelium, a change in the n...

Bart-Pumphrey syndrome is a rare genetic condition that primarily affects the skin, nails, and hearing. The condition is known by several names that r...

Barth syndrome is an inborn error of phospholipid metabolism that primarily affects the heart and skeletal muscles, and is characterized by cardiomyop...

Bartholin gland adenocarcinoma is a type of cancer that begins in the glandular cells of the major vestibular gland. This gland is located near the op...

Bartholin gland adenoid cystic carcinoma is a rare type of cancer that starts in the Bartholin gland. This gland is part of the female reproductive sy...

Bartholin gland adenosquamous carcinoma is a cancer that starts in the Bartholin gland. It is defined by the presence of malignant glandular epithelia...

Bartholin gland small cell carcinoma is a rare neuroendocrine type of cancer that originates in the Bartholin gland. This type of cancer is characteri...

Bartholin gland transitional cell carcinoma is a rare type of cancer that starts in the Bartholin gland. It is characterized by the presence of malign...