Choroid spindle cell melanoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Christianson syndrome is a very rare condition that mainly affects the brain and body development. It is a type of syndromic intellectual disability c...

CHRNG-associated hypo-akinesia disorder of prenatal onset is a rare condition that arises from changes in both copies of the CHRNG gene. These changes...

Chromomycosis is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited. It is a chronic cutane...

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

Chromophobe renal cell carcinoma is a rare subtype of kidney cancer that originates in the intercalating cells of the collecting ducts. It typically m...

Chromosomal disorders refer to conditions caused by an abnormal chromosome constitution. This means that there is either extra or missing chromosome m...

Chromosome 10 disorder is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Chromosome 10q23 deletion syndrome is a rare condition characterized by a partial monosomy affecting the 10q22.3q23.3 region. Clinically, it presents...

Chromosome 11 disorder is a condition characterized by structural or numerical abnormalities affecting chromosome 11. Because the precise genetic caus...

Chromosome 11p13 deletion syndrome, distal, is characterized by an autosomal dominant inheritance pattern. While the specific genetic basis has not be...

Chromosome 11q trisomy is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Chromosome 12 disorder is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Chromosome 12p deletion is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Chromosome 13 disorder is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

chromosome 13p duplication is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Chromosome 13q14 deletion syndrome is characterized by a partial deletion of the long arm of chromosome 13, leading to various developmental and physi...

Chromosome 13q33-q34 deletion syndrome is characterized by a range of clinical features, primarily associated with abnormal facial morphology and hypo...

chromosome 13q-mosaicism is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

chromosome 13q trisomy is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.