Childhood testicular mixed embryonal carcinoma and teratoma is an extremely rare condition. Because few cases have been documented, detailed clinical...

Childhood testicular mixed germ cell cancer is an extremely rare condition. Because few cases have been documented, detailed clinical information is l...

childhood vagina botryoid rhabdomyosarcoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is li...

CHILD syndrome, also known as Congenital Hemidysplasia with Ichthyosiform nevus and Limb Defects (CS), is a rare genetic condition. It is inherited in...

CHIME syndrome is a rare condition that affects several parts of the body, including the eyes, heart, skin, and brain. It is classified as an ectoderm...

Choanal atresia (CA) is a congenital condition characterized by the obstruction of one or both choanal apertures, leading to varying degrees of respir...

Choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome is a very rare multisystem condition that primarily affects structures o...

Choanal atresia, bilateral is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome, also called Burn-McKeown syndrome, is an extremely rare inherited cond...

Choanal atresia, unilateral is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Cholangiocarcinoma is a type of cancer that originates in the bile ducts, including those within the liver (intrahepatic cholangiocarcinoma) and at th...

Cholangiocarcinoma, susceptibility to is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited...

Cholangiolocellular carcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited. It is...

Cholera is an infectious disease caused by the bacterium Vibrio cholerae. It is characterized by severe watery diarrhea, which can lead to dehydration...

Cholestasis, intrahepatic, of pregnancy, type 1 (ICP1) is associated with variants in the ATP8B1 gene, which is inherited in an autosomal dominant man...

Cholestasis, intrahepatic, of pregnancy, type 3 (ICP3) is associated with genetic variants in the ABCB4 gene, which is known to play a role in bile tr...

Cholestasis-pigmentary retinopathy-cleft palate syndrome, also known as Hardikar syndrome, is a congenital disorder that affects multiple organ system...

Cholestasis, progressive familial intrahepatic, 10 is a condition affecting the liver that leads to impaired bile flow and progressive liver dysfuncti...

Cholestasis, progressive familial intrahepatic, 11 (PFIC11) is associated with genetic variants in the SEMA7A gene and follows an autosomal recessive...

Cholestasis, progressive familial intrahepatic, 12 is a disorder primarily affecting liver function with disturbances in bile flow. The condition is g...