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56,125 results found
You searched for “X” in All. RX Search found 56,125 result(s) and checks doctor-selected, exact-title, synonym, and related matches.
Autosomal recessive severe congenital neutropenia (SCN) due to C-X-C motif chemokine receptor 2 (CXCR2) deficiency is a very rare, inherited immune disorder. Babies are born with...
Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency is a very rare, inherited immune disorder present from infancy. Children are born with chronically low neutrophils—the...
Progressive external ophthalmoplegia (PEO) is a mitochondrial muscle condition where the muscles that move the eyes slowly become weak. Over years, people develop droopy eyelids (ptosis)...
Autosomal recessive progressive external ophthalmoplegia is a rare, inherited mitochondrial muscle disease. “External ophthalmoplegia” means the eye-moving muscles slowly become weak, so the eyelids droop (ptosis)...
Autosomal Recessive Primary Immunodeficiency with Defective Spontaneous Natural Killer (NK) Cell Cytotoxicity is a genetic immune disorder that runs in families in an autosomal recessive way....
TMEM126A-related optic atrophy (with or without extra-ocular features) is a rare inherited eye and nerve condition. It mainly damages the optic nerves—the “cables” that carry visual...
SYNE1-related arthrogryposis multiplex congenita is a rare, inherited, muscle-based condition where a baby is born with stiff joints (contractures) in multiple body areas. It happens because...
Autosomal recessive myogenic arthrogryposis multiplex congenita is a rare, inherited condition in which a baby is born with stiff joints in two or more body areas...
Autosomal recessive limb-girdle muscular dystrophy type 2X (LGMD2X) is a rare, inherited muscle disease. It mainly weakens the muscles around the hips, thighs, shoulders, and upper...
Tyrosine hydroxylase–deficient dopa-responsive dystonia is a rare, inherited movement disorder. It happens because the TH gene does not work properly. The TH gene makes the tyrosine...
Severe infantile axonal neuropathy with respiratory failure type 1 is a very rare inherited nerve disease that begins in early infancy. It mainly damages the long...
Autosomal recessive cutis laxa type 2, progeroid type is a rare genetic condition that makes the skin loose and wrinkled and also affects many body systems....
