Lethal congenital contracture syndrome 1 (LCCS1), also called Multiple contracture syndrome, Finnish type, is an autosomal recessive genetic disorder...

syndrome Lenz–Majewski syndrome Leriche's syndrome Leschke syndrome Lesch–Nyhan syndrome Lethal congenital contracture syndrome Lethal white syndrome...

Arthrogryposis (AMC) describes congenital joint contracture in two or more areas of the body. It derives its name from Greek, literally meaning 'curving...

congenital, nongoitrous Ito hypomelanosis Joubert syndrome Keipert syndrome Legius syndrome LEOPARD syndrome Lethal congenital contracture syndrome MASA...

meningocele syndrome Legius syndrome Lethal congenital contracture syndrome 1, 2, 7, and 9 Lethal Kniest-like syndrome Lethal multiple pterygium syndrome Lissencephaly...

Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies...

Noonan syndrome (NS) is a genetic disorder that may present with mildly unusual facial features, short height, congenital heart disease, bleeding problems...

dyschondrosteosis Lesch–Nyhan syndrome Lethal chondrodysplasia Moerman type Lethal chondrodysplasia Seller type Lethal congenital contracture syndrome Letterer–Siwe disease...

Hallermann–Streiff syndrome is a congenital disorder that affects growth, cranial development, hair-growth, and dental development. There are fewer than...

basal cell carcinoma syndrome hereditary hemorrhagic telangiectasia lethal congenital contracture syndrome nail-patella syndrome (NPS) nonsyndromic deafness...