Kosmix
One sec... we're building your guide for
Smith-lemli-opitz Syndrome
Smith-Lemli-Opitz syndrome
Overview
Anatomy
Health Providers & Organizations
Main ›
Anatomy ›
Health Providers & Organizations ›
Anatomy
›
Body Maps
Layers:
(click to view/hide)
+
Zoom
-
Search:
Related in the Kosmos
?
Inborn errors of metabolism
Glutaricaciduria
Leukodystrophy, globoid cell
SCAD deficiency
Galactosemias
Steroid sulfatase deficiency
Phenylketonuria
Autosomal recessive disorders
(10)
Shwachman syndrome
Ablepharon macrostomia syndrome
Carpenter syndrome
Chondroectodermal dysplasia
Adducted thumb syndrome
Adducted thumb syndrome
Meckel syndrome
Cerebrotendinous xanthomatosis
Leukodystrophy, globoid cell
SCAD deficiency
Phenylketonuria
more...
Genetic disorders
(43)
Polydactyly
Trisomy 13
Microcephaly
Hyperostosis, cortical, congenital
Trisomy 18
Trisomy 18
Adrenoleuk- odystrophy
Laurence-Moon-Biedl syndrome
Hereditary sensory and autonomic neuropathies
Rubinstein-taybi syndrome
Smith-Magenis syndrome
Thrombocytopenia absent radius
Turner syndrome
Noonan syndrome
Laurence Moon syndrome
Hallerman-Streiff Syndrome
Pallister-Hall syndrome
VATER syndrome
Robinow syndrome
Williams syndrome
Spondyloep- imetaphyseal dysplasia, Strudwick type
Shprintzen syndrome
Multiple hereditary exostoses
Aarskog-Scott syndrome
Simpson-Go- labi-Behmel syndrome
Chromosome abnormalities
Cri du chat syndrome
Popliteal pterygium syndrome
Cornelia de Lange syndrome
Langer-giedion syndrome
4p- syndrome
Stickler syndrome
Glutaricaciduria
Leukodystrophy, globoid cell
Shwachman syndrome
Ablepharon macrostomia syndrome
SCAD deficiency
Galactosemias
Carpenter syndrome
Chondroectodermal dysplasia
Adducted thumb syndrome
Meckel syndrome
Cerebrotendinous xanthomatosis
Phenylketonuria
more...
Congenital disorders
(8)
Seckel syndrome
Persistent thyroglossal duct
Hypospadias
Malformations
Holoprosencephaly
Holoprosencephaly
Genetic disorders
Polydactyly
Microcephaly
more...
Obstetrics
Fetofetal transfusion
Prenatal diagnosis
Steroid sulfatase deficiency
Diseases and disorders
(14)
Hydrolethalus syndrome
Lupus erythematosus, cutaneous
Growth retardation
Skeletal dysplasia
Hypoplasia
Hypoplasia
Weaver syndrome
X-linked hypophosphatemic rickets
Short rib-polydactyly syndrome
Leukodystrophy, globoid cell
Seckel syndrome
Ablepharon macrostomia syndrome
Hallerman-Streiff Syndrome
VATER syndrome
Cerebrotendinous xanthomatosis
more...
Syndromes
(24)
Sotos syndrome
Silver-Russell dwarfism
Swyer syndrome
Syndrome
Trisomy 13
Trisomy 13
Fetofetal transfusion
Trisomy 18
Hereditary sensory and autonomic neuropathies
Ablepharon macrostomia syndrome
Smith-Magenis syndrome
Turner syndrome
Noonan syndrome
Carpenter syndrome
Hallerman-Streiff Syndrome
Robinow syndrome
Chondroectodermal dysplasia
Williams syndrome
Adducted thumb syndrome
Shprintzen syndrome
Aarskog-Scott syndrome
Cri du chat syndrome
Cornelia de Lange syndrome
4p- syndrome
Stickler syndrome
more...
Medical condition
(68)
Opitz syndrome
Rsh syndrome
Syndactyly
Craniofrontonasal dysplasia
Glossopharyngeal nerve diseases
Glossopharyngeal nerve diseases
Floating harbor syndrome
Type i complex regional pain syndrome
Myopathies, structural, congenital
Enterocolitis, pseudomembranous
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Asphyxiating thoracic dystrophy
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Congenital aganglionic megacolon
Intervertebral disk displacement
Rosenthal syndrome
Brachial plexus neuropathies
Spongioblastoma
Central hypoventilation syndrome
Hypoplastic left heart syndrome
Mental deficiency
Polydactyly
Trisomy 13
Microcephaly
Fetofetal transfusion
Glutaricaciduria
Leukodystrophy, globoid cell
Shwachman syndrome
Hydrolethalus syndrome
Hyperostosis, cortical, congenital
Sotos syndrome
Purpura, schoenlein-henoch
Trisomy 18
Laurence-Moon-Biedl syndrome
Hereditary sensory and autonomic neuropathies
Ablepharon macrostomia syndrome
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Olfaction disorders
Thrombocytopenia absent radius
Galactosemias
Skeletal dysplasia
Noonan syndrome
Steroid sulfatase deficiency
Carpenter syndrome
Pallister-Hall syndrome
Sitosterolemia
VATER syndrome
Hypospadias
Robinow syndrome
Chondroectodermal dysplasia
Spondyloep- imetaphyseal dysplasia, Strudwick type
Adducted thumb syndrome
Optic neuropathy, ischemic
Shprintzen syndrome
Multiple hereditary exostoses
Aarskog-Scott syndrome
Chromosome abnormalities
Cri du chat syndrome
Popliteal pterygium syndrome
Swyer syndrome
Cerebrotendinous xanthomatosis
Cornelia de Lange syndrome
Short rib-polydactyly syndrome
Langer-giedion syndrome
Phenylketonuria
Stickler syndrome
more...
See also
(18)
Congenital disorders
DHCR7
Purpura, schoenlein-henoch
Am. J. Med. Genet.
7-Dehydroc- holesterol
7-Dehydroc- holesterol
Polyendocr- inopathies, autoimmune
Olfaction disorders
Sterol
Sitosterolemia
David Weyhe Smith
Optic neuropathy, ischemic
RET oncogene
Hallervorden-spatz syndrome
Autosomal recessive
Short stature
Sonic hedgehog
Cockayne syndrome
Dubowitz syndrome
more...
more categories...
Health Providers & Organizations
›
Vitals.com
