Connective Tissue Disorders

Aortic valve disease 1
Arterial tortuosity syndrome
Bone mineral density QTL18 - osteoporosis
Brittle cornea syndrome
Bruck syndrome
Congenital contractural arachnodactyly
Cutis laxa - autosomal dominant
Cutis laxa - autosomal recessive - type IIB
Cutis laxa autosomal dominant 2
Cutis laxa autosomal recessive - Cutis laxa type IA
Cutis laxa autosomal recessive - Cutis laxa type IB
Cutis laxa autosomal recessive - Cutis laxa type IC
Ectopia lentis
Ehlers-Danlos syndrome - EDS
Ehlers-Danlos syndrome kyphoscoliotic type
Ehlers-Danlos syndrome type I - classic type
Ehlers-Danlos syndrome type II - classic type
Ehlers-Danlos syndrome vascular type
Ehlers-Danlos syndrome with progressive kyphoscoliosis myopathy and hearing loss
Geleophysic dysplasia
Homocystinuria
Hypophosphatasia
Kniest dysplasia
Larsen syndrome
Loeys-Dietz syndrome type 1A
Loeys-Dietz syndrome type 1B
Loeys-Dietz syndrome type 2A
Loeys-Dietz syndrome type 2B
Loeys-Dietz syndrome type 3 - aneurysms-osteoarthritis syndrome
Loeys-Dietz syndrome type 4
Lysyl hydroxylase 3 deficiency
Marfan Syndrome
Marshall syndrome
Metaphyseal chondrodysplasia Schmid type
Multiple epiphyseal dysplasia
Multiple joint dislocations short stature craniofacial dysmorphism and congenital heart defects
Multiple self-healing squamous epithelioma
Osteogenesis imperfecta
Osteogenesis imperfecta type IX
Osteogenesis imperfecta type V
Osteogenesis imperfecta type VIII
Osteogenesis imperfecta type X
Osteogenesis imperfecta type XII
Osteoporosis - early onset
$Osteoporosis with fractures$
Osteoporosis with fractures
Osteoporosis-pseudoglioma syndrome
Otospondylomegaepiphyseal dysplasia
Porencephaly
Spondylocheirodysplasia
Spondyloepiphyseal dysplasia congenita
Stickler syndrome
Supravalvular aortic stenosis
Thoracic Aortic Aneurysm with Dissection - TAAD
van den Ende-Gupta syndrome
Wagner syndrome
Weill-Marchesani syndrome
Weissenbacher-Zweymuller syndrome

Aortic valve disease 1

Arterial tortuosity syndrome

Bone mineral density QTL18 - osteoporosis

Brittle cornea syndrome

Bruck syndrome

Congenital contractural arachnodactyly

Cutis laxa - autosomal dominant

Cutis laxa - autosomal recessive - type IIB

Cutis laxa autosomal dominant 2

Cutis laxa autosomal recessive - Cutis laxa type IA

Cutis laxa autosomal recessive - Cutis laxa type IB

Cutis laxa autosomal recessive - Cutis laxa type IC

Ectopia lentis

Ehlers-Danlos syndrome - EDS

Ehlers-Danlos syndrome kyphoscoliotic type

Ehlers-Danlos syndrome type I - classic type

Ehlers-Danlos syndrome type II - classic type

Ehlers-Danlos syndrome vascular type

Ehlers-Danlos syndrome with progressive kyphoscoliosis myopathy and hearing loss

Geleophysic dysplasia

Homocystinuria

Hypophosphatasia

Kniest dysplasia

Larsen syndrome

Loeys-Dietz syndrome type 1A

Loeys-Dietz syndrome type 1B

Loeys-Dietz syndrome type 2A

Loeys-Dietz syndrome type 2B

Loeys-Dietz syndrome type 3 - aneurysms-osteoarthritis syndrome

Loeys-Dietz syndrome type 4

Lysyl hydroxylase 3 deficiency

Marfan Syndrome

Marshall syndrome

Metaphyseal chondrodysplasia Schmid type

Multiple epiphyseal dysplasia

Multiple joint dislocations short stature craniofacial dysmorphism and congenital heart defects

Multiple self-healing squamous epithelioma

Osteogenesis imperfecta

Osteogenesis imperfecta type IX

Osteogenesis imperfecta type V

Osteogenesis imperfecta type VIII

Osteogenesis imperfecta type X

Osteogenesis imperfecta type XII

Osteoporosis - early onset

Osteoporosis with fractures

Osteoporosis-pseudoglioma syndrome

Otospondylomegaepiphyseal dysplasia

Porencephaly

Spondylocheirodysplasia

Spondyloepiphyseal dysplasia congenita

Stickler syndrome

Supravalvular aortic stenosis

Thoracic Aortic Aneurysm with Dissection - TAAD

van den Ende-Gupta syndrome

Wagner syndrome

Weill-Marchesani syndrome

Weissenbacher-Zweymuller syndrome