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Opitz Syndrome
Opitz syndrome
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Diseases and disorders
(69)
Opitz trigonocephaly syndrome
Autosomal dominant opitz G/BBB syndrome
Rsh syndrome
Frias syndrome
Polydactyly
Polydactyly
Glutaricaciduria
Syndactyly
Microcephaly
Noonan syndrome
Craniofrontonasal dysplasia
Floating harbor syndrome
Trisomy 13
Hypospadias
Sotos syndrome
Shwachman syndrome
Fetofetal transfusion
Oculo dento digital dysplasia
Skeletal dysplasia
Hypertelorism with esophageal abnormality and hypospadias
Glossopharyngeal nerve diseases
Hyperostosis, cortical, congenital
Laurence-Moon-Biedl syndrome
Hydrolethalus syndrome
Apert syndrome
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Leukodystrophy, globoid cell
Osteogenesis imperfecta
Enterocolitis, pseudomembranous
Hereditary sensory and autonomic neuropathies
Physiologic nystagmus
Trisomy 18
Histiocytosis non-langerhans-cell
Growth retardation
Thrombocytopenia absent radius
Polyendocr- inopathies, autoimmune
Cayler syndrome
Lupus erythematosus, cutaneous
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Sturge-weber syndrome
Ablepharon macrostomia syndrome
Seckel syndrome
Intervertebral disk displacement
Asphyxiating thoracic dystrophy
X-linked hypophosphatemic rickets
Rosenthal syndrome
Hypoplasia
Uveomening- oencephalitic syndrome
Spondyloep- imetaphyseal dysplasia, Strudwick type
Chondroectodermal dysplasia
Weaver syndrome
Carpenter syndrome
Adducted thumb syndrome
VATER syndrome
Brachial plexus neuropathies
Stickler syndrome
Optic neuropathy, ischemic
Galactosemias
Robinow syndrome
Androgen insensitivity syndrome
Ollier disease
Spinal muscular atrophy
Monosomy 9p
Pallister-Hall syndrome
Spongioblastoma
Multiple hereditary exostoses
more...
Inborn errors of metabolism
Smith-lemli-opitz syndrome
Short chain acyl coenzyme A dehydrogenase deficiency
Glutaricaciduria
Leukodystrophy, globoid cell
Galactosemias
Autosomal recessive disorders
(10)
Otospondyl- omegaepiphyseal dysplasia
Smith-lemli-opitz syndrome
Shwachman syndrome
Oculo dento digital dysplasia
Leukodystrophy, globoid cell
Leukodystrophy, globoid cell
Ablepharon macrostomia syndrome
Chondroectodermal dysplasia
Short chain acyl coenzyme A dehydrogenase deficiency
Carpenter syndrome
Adducted thumb syndrome
more...
Congenital disorders
(8)
Genetic disorders
Holoprosencephaly
Congenital anomaly
Opitz trigonocephaly syndrome
Polydactyly
Polydactyly
Microcephaly
Hypospadias
Seckel syndrome
more...
Genetic disorder
(8)
Opitz-Kaveggia syndrome
Mulibrey nanism
Simpson-Go- labi-Behmel syndrome
Laurence Moon syndrome
Cayler syndrome
Cayler syndrome
Ablepharon macrostomia syndrome
Short chain acyl coenzyme A dehydrogenase deficiency
Adducted thumb syndrome
more...
Genodermatoses
Turner syndrome
Hallerman-Streiff Syndrome
Noonan syndrome
Apert syndrome
Genetic disorders
(45)
Smith-Magenis syndrome
Rubinstein-taybi syndrome
Adrenoleuk- odystrophy
Trisomy
Smith-lemli-opitz syndrome
Smith-lemli-opitz syndrome
Opitz-Kaveggia syndrome
Autosomal dominant opitz G/BBB syndrome
Polydactyly
Glutaricaciduria
Microcephaly
Noonan syndrome
Trisomy 13
Shwachman syndrome
Oculo dento digital dysplasia
Hyperostosis, cortical, congenital
Turner syndrome
Laurence-Moon-Biedl syndrome
Apert syndrome
Leukodystrophy, globoid cell
Osteogenesis imperfecta
Mulibrey nanism
Hereditary sensory and autonomic neuropathies
Trisomy 18
Thrombocytopenia absent radius
Cayler syndrome
Simpson-Go- labi-Behmel syndrome
Ablepharon macrostomia syndrome
Spondyloep- imetaphyseal dysplasia, Strudwick type
Chondroectodermal dysplasia
Short chain acyl coenzyme A dehydrogenase deficiency
Carpenter syndrome
Adducted thumb syndrome
VATER syndrome
Stickler syndrome
Hallerman-Streiff Syndrome
Galactosemias
Robinow syndrome
Androgen insensitivity syndrome
Williams syndrome
Laurence Moon syndrome
Spinal muscular atrophy
Pallister-Hall syndrome
Multiple hereditary exostoses
Genetic disorder
Otospondyl- omegaepiphyseal dysplasia
more...
See also
(15)
DHCR7
Am. J. Med. Genet.
Telecanthus
MID1
BBBG
BBBG
Mosaicism
Syndrome
7-dehydroc- holesterol
Autosomal recessive
Russel-Silver Syndrome
Short stature
Developmental disorder
Williams syndrome
Hydantoin
Chromosome 22
more...
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