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Antley-bixler Syndrome
Antley-Bixler syndrome
Overview
Anatomy
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Autosomal recessive disorders
Fibrochondrogenesis
Atelosteogenesis, type II
Raine syndrome
Otospondyl- omegaepiphyseal dysplasia
21 hydroxylase deficiency
Diastrophic dysplasia
Adrenal hyperplasia, congenital
Syndromes
(10)
Pfeiffer syndrome
Maffucci syndrome
Crouzon syndrome
Jackson-Weiss syndrome
Apert syndrome
Apert syndrome
Androgen insensitivity syndrome
Saethre-Chotzen syndrome
Kallmann syndrome
Syndrome
Raine syndrome
more...
Rare diseases
(8)
Boomerang dysplasia
Hereditary multiple exostoses
Thanatophoric dysplasia
Arthrogryposis
Fibrochondrogenesis
Fibrochondrogenesis
Atelosteogenesis, type II
Raine syndrome
Saethre-Chotzen syndrome
more...
Genetic disorders
(28)
Estrogen insensitivity syndrome
Hyperimmun- oglobulinemia D with recurrent fever
Apparent mineralocorticoid excess syndrome
Acrocephal- opolysyndactyly
Spondyloepiphyseal dysplasia congenita
Spondyloepiphyseal dysplasia congenita
Hypochondrogenesis
Achondroplasia
Andersen disease
Loeys dietz syndrome
Hypochondroplasia
Arachnodactyly
Fibrochondrogenesis
Atelosteogenesis, type II
Boomerang dysplasia
Raine syndrome
Otospondyl- omegaepiphyseal dysplasia
Pfeiffer syndrome
Crouzon syndrome
Jackson-Weiss syndrome
Apert syndrome
Hereditary multiple exostoses
Androgen insensitivity syndrome
Saethre-Chotzen syndrome
Thanatophoric dysplasia
Kallmann syndrome
21 hydroxylase deficiency
Diastrophic dysplasia
Adrenal hyperplasia, congenital
more...
Congenital disorders
(8)
Achondrogenesis type 1B
Achondrogenesis type 2
Achondrogenesis
Congenital malformations
Choanal atresia
Choanal atresia
Fibrochondrogenesis
Saethre-Chotzen syndrome
Arthrogryposis
more...
Genodermatoses
Chondrodysplasia punctata, rhizomelic
Aplasia cutis congenita
X-linked ichthyosis
Acrocephal- opolysyndactyly
Pfeiffer syndrome
Crouzon syndrome
Apert syndrome
Metabolism
Cytochrome P450
Inborn error of metabolism
Virilization
Skeletal disorders
Ollier disease
Craniosynostosis
Hereditary multiple exostoses
Clusters of differentiation
FGFR2
FGFR3
FGFR1
Diseases and disorders
(51)
Schmid metaphyseal chondrodysplasia
Hydrops-ectopic calcificat- ion-moth-eaten skeletal dysplasia
Osteochondropathy
Chondromatous
Osteochond- rodysplasia
Osteochond- rodysplasia
Short rib-polydactyly syndrome
Camurati engelmann disease
Anonychia onychodystrophy
Lathosterolosis
Osteopoikilosis
17 beta-hydroxysteroid dehydrogenase deficiency
Metaphyseal dysplasia
Acanthoche- ilonemiasis
Agenesis of corpus callosum
Ambiguous genitalia
Enchondromatosis
Synostosis
Anemia, hemolytic
Aniridia
Dysostosis
Fibrochondrogenesis
Boomerang dysplasia
Raine syndrome
Chondrodysplasia punctata, rhizomelic
Achondrogenesis type 2
Apparent mineralocorticoid excess syndrome
Acrocephal- opolysyndactyly
Ollier disease
Spondyloepiphyseal dysplasia congenita
Hypochondrogenesis
Achondroplasia
Maffucci syndrome
Crouzon syndrome
Apert syndrome
Aplasia cutis congenita
Hereditary multiple exostoses
Androgen insensitivity syndrome
Andersen disease
X-linked ichthyosis
Saethre-Chotzen syndrome
Thanatophoric dysplasia
Kallmann syndrome
Craniosynostosis
Hypochondroplasia
Diastrophic dysplasia
Granulomatosis
Arachnodactyly
Adrenal hyperplasia, congenital
Inborn error of metabolism
Astrocytoma
Arthrogryposis
more...
See also
(20)
Diseases and disorders
P450 oxidoreductase
Steroid metabolism
5 alpha reductase deficiency
alopecia cicatrisata
alopecia cicatrisata
Autosomal recessive
Acanthocytosis
Osseous
Brian Bixler
Autosomal dominant
17 alpha hydroxylase deficiency
Androgen receptor
Endocrine pathology
Abscess of thymus
Endocrine disorders
Steroidogenesis
P450c17
7-dehydroc- holesterol
Neoplasia
Craniofacial
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