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Chronic diarrhea is defined as the passage of loose or liquid stools, watery stools three or more times a day for at least 4…
You searched for “Y” in All. RX Search found 56,145 result(s) and checks doctor-selected, exact-title, synonym, and related matches.
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a long-lasting disease where the body’s own immune system attacks the covering of the nerves (myelin) in the arms, legs...
Prieur–Griscelli syndrome is another name for a very rare disease called neonatal-onset multisystem inflammatory disease (NOMID) or chronic infantile neurologic, cutaneous and articular syndrome (CINCA). It...
Neonatal-onset multisystem inflammatory disease (NOMID) is a very rare genetic disease where the immune system is “over-active” from birth and causes strong, long-lasting inflammation in many...
Infantile-onset multisystem inflammatory disease is a very rare genetic illness where a baby is born with strong, ongoing inflammation in many parts of the body, such...
Chronic neurologic cutaneous and articular syndrome (CINCA syndrome) is a very rare, life-long inflammatory disease that starts in the newborn period or early infancy. It is...
Quie syndrome is another name for a disease called chronic granulomatous disease (CGD). In this disease, some white blood cells that fight germs do not work...
Congenital dysphagocytosis is an old medical name for a serious inherited immune system disease that doctors now call chronic granulomatous disease (CGD). In this disease, some...
Bridges–Good syndrome is another name for a rare illness called chronic granulomatous disease (CGD). In this disease, some white blood cells (called phagocytes) cannot make important...
Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (usually shortened to “CEAS” or “chronic enteropathy associated with SLCO2A1”) is a rare...
Chronic enteropathy associated with SLCO2A1 gene (CEAS) is a rare inherited bowel disease in which many long-lasting small ulcers form in the small intestine, especially in...
CBL-mutated juvenile myelomonocytic leukemia is a rare blood cancer that happens in babies and young children when the CBL gene is damaged (mutated) in their blood-forming...
NF1-associated juvenile myelomonocytic leukemia (NF1-JMML) is a rare blood cancer that happens in young children who already have neurofibromatosis type 1 (NF1). In this disease, early...
