Craniofrontonasal syndrome is an X-linked malformation condition primarily affecting craniofacial and skeletal development. It is caused by pathogenic...

Craniolenticulosutural dysplasia, also known as Boyadjiev-Jabs syndrome or CLSD, is a condition affecting craniofacial development and the skeleton. I...

Craniometadiaphyseal dysplasia, wormian bone type is an extremely rare disorder affecting the development of the cranial and tubular bones. It is char...

Craniometaphyseal dysplasia is a very rare bone disorder characterized by abnormal thickening of the cranial bones and widening of the metaphyses in l...

Craniometaphyseal dysplasia, autosomal dominant is a skeletal condition that primarily affects the craniofacial bones and dentition. It is associated...

Craniometaphyseal dysplasia, autosomal recessive is a skeletal disorder marked by abnormal bone development that primarily affects the skull and facia...

Craniomicromelic syndrome is a developmental disorder that primarily affects skeletal formation, especially the skull and limbs. It is characterized b...

Cranio-osteoarthropathy is a form of primary hypertrophic osteoarthropathy characterized by delayed closure of the cranial sutures and fontanels, digi...

Craniopharyngioma is a benign, partly cystic tumor of the sellar region that is believed to originate from Rathke pouch epithelium. Recognized subtype...

Craniorachischisis is the most severe form of neural tube defect characterized by an open brain and spinal cord, resulting in a major congenital malfo...

Craniorhiny is an extremely rare condition with very limited information available about its clinical presentation. It appears to affect individuals a...

Craniosynostosis is characterized by the premature fusion of one or more cranial sutures, leading to abnormal skull shape and potential neurological i...

Craniosynostosis 2 is a syndromic form of craniosynostosis that affects skull development and is characterized by abnormal skull shapes such as fronta...

Craniosynostosis 4 is a condition affecting the development of the skull, resulting in the premature fusion of one or more cranial sutures. This disor...

Craniosynostosis 6 is a congenital condition characterized by the premature fusion of one or more cranial sutures, leading to abnormal skull formation...

Craniosynostosis, Adelaide type is a condition that affects skull development, resulting from the premature fusion of one or more of the skull sutures...

Craniosynostosis alopecia brain defect is a condition that appears to involve abnormal skull development, hair growth, and brain formation. While deta...

Craniosynostosis-anal anomalies-porokeratosis syndrome is a very rare congenital condition that affects multiple systems including the skull, genital...

Craniosynostosis and dental anomalies is a condition characterized by premature fusion of skull sutures and significant dental irregularities. It resu...

Craniosynostosis arthrogryposis cleft palate is a complex congenital condition that affects the shape of the skull, the joints, and the formation of t...