Cleft lip–progressive retinopathy syndrome is a very rare birth condition. In this condition a baby is born with a cleft lip (a gap in the upper lip) and later ...

Cleft lip–cone rod dystrophy syndrome is an extremely rare inherited condition in which a baby is born with a cleft lip, and later in life develops a ...

Cleft lip-retinopathy syndrome is an extremely rare congenital condition in which a baby is born with a cleft lip and later develops a slowly worsening disease ...

Cleft lip and palate–craniofacial dysmorphism–congenital heart defect–deafness (hearing loss) syndrome is a very rare genetic condition. It affects how the ...

Cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome is a very rare genetic condition that changes how a baby’s face, ...

Disease of the cleft of the alveolar process of the maxilla usually means all the problems related to a bony gap in the tooth-bearing part of the upper jaw ...

Cleft lip and alveolus means there is a gap (cleft) in the upper lip and in the gum ridge that holds the upper teeth (alveolar ridge). This gap can be small or ...

Asymmetry of the face and limbs with overgrowth means that one side of the body, or one part such as an arm, leg or part of the face, grows larger than the ...

A lymphatic malformation of the face and neck is a soft, spongy swelling made from lymph vessels that grew in an abnormal way before birth. These vessels form ...

Oculootofacial dysplasia is a very rare genetic condition that affects the eyes (“oculo”), ears (“oto”), and face (“facial”). Children are born with this ...

Burn-McKeown syndrome is a very rare genetic condition present from birth. Children with this syndrome usually have blocked or very narrow back parts of the ...

Branchio-oculo-facial syndrome (often shortened to BOFS) is a rare genetic condition that affects how the face, neck, eyes, and sometimes ears and kidneys form ...

Cerebrooculonasal syndrome (also written cerebro-oculo-nasal syndrome, CONS) is a very rare birth condition where a baby is born with problems in three main ...

Cerebro-costo-mandibular syndrome (CCMS) is a very rare genetic condition that is present from birth. It mainly affects the jaw (mandible), the ribs, and the ...

Cerebral gigantism-jaw cysts syndrome is an extremely rare birth (congenital) condition in which a child has very fast body and head growth (cerebral ...

Cerebellar-facial-dental syndrome (CFDS) is a very rare genetic condition that affects brain development, face shape, and teeth. It is a neurodevelopmental ...

Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural deafness syndrome is a very rare inherited brain and nerve disorder. Doctors often call it ...

CAPOS syndrome is a very rare genetic brain and nerve disease. The name CAPOS comes from five main problems: Cerebellar ataxia (poor balance and coordination), ...

Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome is usually called CAPOS syndrome. It is a very rare genetic brain and ...

Cerebellar ataxia with bilateral vestibular syndrome means that two balance systems are damaged at the same time. The first system is the cerebellum, a part of ...