Disease Directory

Ampulla of vater clear cell adenocarcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is li...

Ampulla of vater mucinous adenocarcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limi...

Ampulla of vater small cell neuroendocrine carcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical informa...

Ampulla of vater squamous cell carcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limi...

Ampullary signet ring cell adenocarcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is lim...

Amyloidosis is a disorder characterized by the abnormal accumulation of amyloid protein in various tissues, which can lead to organ dysfunction. It ca...

Amyloidosis bronchopulmonary is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Amyloidosis cutis dyschromia is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Amyloidosis, hereditary systemic 1 is a multisystem condition characterized primarily by the abnormal deposition of amyloid proteins, with increased c...

Amyloidosis, hereditary systemic 3 is a complex, multi-organ condition characterized by the abnormal deposition of amyloid proteins throughout the bod...

Hereditary systemic amyloidosis type 5 is a multisystem condition characterized by the abnormal deposition of amyloid proteins affecting several organ...

Hereditary systemic amyloidosis 6 is a multi‐system condition characterized by the abnormal deposition of amyloid proteins affecting several organ sys...

Amyloidosis, primary localized cutaneous, 1 is a skin condition characterized by abnormal protein deposits in the skin. It is caused by a mutation in...

Amyloidosis, primary localized cutaneous type 2 (PLCA2) is associated with variants in the IL31RA gene, which is inherited in an autosomal dominant ma...

Primary localized cutaneous amyloidosis type 3 (PLCA3) is associated with variants in the GPNMB gene, which is inherited in an autosomal recessive man...

Amyopathic dermatomyositis is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by the progressive loss of motor neurons in the brain and spinal cor...

Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia is a neurological condition that primarily affects motor function and cogniti...

Amyotrophic lateral sclerosis 27, juvenile is a neuromuscular condition marked by progressive muscle weakness affecting multiple muscle groups. It is...

Amyotrophic lateral sclerosis 28 is a neuromuscular condition that primarily affects motor function, leading to progressive muscle weakness and diffic...