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Adenine Nucleotide Translocator Deficiency
Arthrogryposis and Ectodermal Dysplasia
arthrogryposis due to muscular dystrophy
Arthrogryposis Epileptic Seizures Migrational Brain Disorder
Arthrogryposis Multiplex Congenita 6
Arthrogryposis Multiplex Congenita Whistling Face
arthrogryposis multiplex congenita-1
arthrogryposis multiplex congenita-3
arthrogryposis multiplex congenita-4
arthrogryposis multiplex congenita-5
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death
Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development
Arthrogryposis, Impaired Intellectual Development, and Seizures
ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY
Arthrogryposis, X-Linked, Type V
Bilateral Kienbock's Disease
Bisphosphonate-Associated Osteonecrosis of the Jaw
Boylan Dew Greco Syndrome
Camptodactyly-Ichthyosis Syndrome
CAP-Congenital Myopathy with Arthrogryposis Multiplex Congenita without Heart Involvement
Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome
cerebrooculofacioskeletal syndrome 2
cerebrooculofacioskeletal syndrome 4
chronic progressive external ophthalmoplegia +
Congenital Arthrogryposis with Anterior Horn Cell Disease
congenital fibrosis of the extraocular muscles +
Congenital Neuropathy with Arthrogryposis Multiplex
Cyprus Facial Neuromusculoskeletal Syndrome
distal arthrogryposis type 5
Ehlers-Danlos syndrome musculocontractural type 2
exophthalmic ophthalmoplegia
External Ophthalmoplegia and Myopia
External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation
Familial Static Ophthalmoplegia
fetal akinesia deformation sequence syndrome +
Hamano Tsukamoto Syndrome
hereditary neuropathy with liability to pressure palsies
Holoprosencephaly with Fetal Akinesia/Hypokinesia Sequence
Intellectual Disability with Episodic Ataxia and Congenital Arthrogryposis
internuclear ophthalmoplegia
Jequier Kozlowski Skeletal Dysplasia
Johnston Aarons Schelley Syndrome
Ladda Zonana Ramer syndrome
lethal congenital contracture syndrome +
Massa Casaer Ceulemans Syndrome
Miles-Carpenter syndrome +
Minicore Myopathy, Antenatal Onset, with Arthrogryposis
mitochondrial DNA depletion syndrome 11
Motor Neuron Disease with Dementia and Ophthalmoplegia
Multiple Pterygium Syndrome, Lethal Type
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES
neurogenic-type arthrogryposis multiplex congenita-2
Ocular Myopathy with Curare Sensitivity
Ophthalmoplegia Totalis with Ptosis and Miosis
OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES
Ophthalmoplegia, Familial Total, with Iris Transillumination
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy
Pelvic Dysplasia Arthrogryposis of Lower Limbs
POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS
Progressive External Ophthalmoplegia with Hypogonadism
Progressive Ophthalmoplegia with Scrotal Tongue and Mental Deficiency
progressive supranuclear palsy +
proximal myopathy and ophthalmoplegia
Ray Peterson Scott Syndrome
Schimke X-Linked Mental Retardation Syndrome
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
Spondylohypoplasia, Arthrogryposis and Popliteal Pterygium
Spranger Schinzel Myers Syndrome
Treft Sanborn Carey Syndrome
Ventriculomegaly and Arthrogryposis
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