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Cornelia De Lange Syndrome
Cornelia de Lange Syndrome
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Syndromes
(22)
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Aarskog-Scott syndrome
Zimmerman Laband syndrome
Zimmerman Laband syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Silver-Russell dwarfism
Apert syndrome
Carpenter syndrome
Hereditary sensory and autonomic neuropathies
Fetofetal transfusion
Noonan syndrome
Trisomy 18
Crow-Fukase syndrome
Angelman syndrome
Congenital facial diplegia
22q11.2
Syndrome
Robinow syndrome
more...
Genetic disorders
(42)
Sakati-Nyh- an-Tisdale syndrome
Acrocephal- osyndactylia
Branchio-Oto-Renal Syndrome
Laurence Moon syndrome
Timothy syndrome
Timothy syndrome
Bardet Biedl Syndrome
Hyperostosis, cortical, congenital
Microcephaly
Adrenoleuk- odystrophy
Charcot-Marie Tooth Disease
Crouzonode- rmoskeletal syndrome
Cerebrohepatorenal syndrome
Leukodystrophy, globoid cell
Glutaricaciduria
Beckwith wiedemann syndrome
Vacterl association
Smith-lemli-opitz syndrome
Galactosemias
Tuberous sclerosis
Spondyloep- imetaphyseal dysplasia, Strudwick type
Coffin-lowry syndrome
Polydactyly
Cerebrotendinous xanthomatosis
Multiple hereditary exostoses
Costello syndrome
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Aarskog-Scott syndrome
Zimmerman Laband syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Apert syndrome
Carpenter syndrome
Hereditary sensory and autonomic neuropathies
Noonan syndrome
Trisomy 18
Angelman syndrome
22q11.2
Robinow syndrome
more...
Diseases and disorders
(71)
Craniofrontonasal dysplasia
Syndactyly
Floating harbor syndrome
Chromosome 9 trisomy
Chromosome 5p- syndrome
Chromosome 5p- syndrome
Glossopharyngeal nerve diseases
Weaver syndrome
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Seckel syndrome
Cystathionine beta-synthase deficiency disease
Enterocolitis, pseudomembranous
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Congenital arthromyodysplasia
Ehlers-danlos syndrome dermatosparaxis type
Chromosome 5 trisomy 5p
Intervertebral disk displacement
Rosenthal syndrome
Fryns syndrome
Brachial plexus neuropathies
Rare diseases
Optic neuropathy, ischemic
Cleft palate
Growth retardation
Sakati-Nyh- an-Tisdale syndrome
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Aarskog-Scott syndrome
Acrocephal- osyndactylia
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Branchio-Oto-Renal Syndrome
Apert syndrome
Timothy syndrome
Bardet Biedl Syndrome
Carpenter syndrome
Hyperostosis, cortical, congenital
Microcephaly
Charcot-Marie Tooth Disease
Cerebrohepatorenal syndrome
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Fetofetal transfusion
Glutaricaciduria
Noonan syndrome
Beckwith wiedemann syndrome
Trisomy 18
Vacterl association
Crow-Fukase syndrome
Galactosemias
Angelman syndrome
Tuberous sclerosis
Congenital facial diplegia
Spondyloep- imetaphyseal dysplasia, Strudwick type
Coffin-lowry syndrome
22q11.2
Polydactyly
Robinow syndrome
Cerebrotendinous xanthomatosis
Multiple hereditary exostoses
Costello syndrome
more...
Genetic disorder
(10)
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Acrocephal- osyndactylia
Zimmerman Laband syndrome
Zimmerman Laband syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Branchio-Oto-Renal Syndrome
Laurence Moon syndrome
more...
Rare diseases
(16)
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Aarskog-Scott syndrome
Zimmerman Laband syndrome
Zimmerman Laband syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Carpenter syndrome
Cerebrohepatorenal syndrome
Leukodystrophy, globoid cell
Crow-Fukase syndrome
Angelman syndrome
Robinow syndrome
Multiple hereditary exostoses
more...
Autosomal recessive disorders
(10)
Adducted thumb syndrome
Ablepharon macrostomia syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Yunis Varon syndrome
Donohue syndrome
Carpenter syndrome
Leukodystrophy, globoid cell
Smith-lemli-opitz syndrome
Cerebrotendinous xanthomatosis
more...
Facial features
Synophrys
Philtrum
Cleft palate
Leukodystrophies
Adrenoleuk- odystrophy
Alexander disease
Canavan disease
Cerebrohepatorenal syndrome
Leukodystrophy, globoid cell
Metachromatic leukodystrophy
Pelizaeus-- Merzbacher disease
See also
(20)
NIPBL
Community Development & Leadership Summit
SMC1A
Chromosome 18
Am. J. Med. Genet.
Am. J. Med. Genet.
Persistent thyroglossal duct
Typus
SMC3
Dubowitz syndrome
The International League of Dermatological Societies
Turner syndrome
John E. Lange
Marilyn Lange
Array CGH
Skeletal abnormalities
Corneal dystrophy
A. Lange & Sohne
Autosomal dominant
Hydantoin
Chromosome 3
more...
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