| Disease Browser
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Parent Node:
 Abnormalities, Multiple (D000015) |
Parent Node:
Craniosynostoses (D003398) |
..Starting node
.. Craniosynostosis Syndrome, Autosomal Recessive (C564700)
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Child Nodes:
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Sister Nodes: |
..Acrocephalosyndactylia (D000168)  11
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..Aurocephalosyndactyly (C566235)
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..Baraitser Rodeck Garner syndrome (C537906)
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..Bohring syndrome (C537419)
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..C SYNDROME (OMIM:211750)
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..Calabro syndrome (C537960)
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..Cole Carpenter syndrome (C535963)
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..Cranioectodermal Dysplasia (C562966) 1
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..Craniometaphyseal dysplasia, autosomal recessive type (C536570)
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..Craniosynostosis Mental Retardation Clefting Syndrome (C565663)
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..Craniosynostosis Microcephaly with Chromosomal Breakage and Other Abnormalities (C565667)
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..Craniosynostosis radial aplasia syndrome (C536788)
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..Craniosynostosis Syndrome, Autosomal Recessive (C564700)
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..Craniosynostosis with Anomalies of the Cranial Base and Digits (C565666)
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..Craniosynostosis with Ectopia Lentis (C566357)
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..Craniosynostosis with Fibular Aplasia (C565665)
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..Craniosynostosis with Ocular Abnormalities and Hallucal Defects (C564263)
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..Craniosynostosis, Adelaide Type (C563471)
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..Craniosynostosis, anal anomalies, and porokeratosis (C536789)
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..Craniosynostosis, Calcification of Basal Ganglia, and Facial Dysmorphism (C564241)
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..Craniosynostosis, Philadelphia Type (C563368)
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..Craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus (C536790)
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..Craniosynostosis, Type 2 (C565753)
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..Craniosynostosis-Mental Retardation Syndrome of Lin and Gettig (C565664)
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..Craniotelencephalic dysplasia (C535597)
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..Cutis Gyrata Syndrome of Beare And Stevenson (C565129)
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..Fine-Lubinsky syndrome (C537933)
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..FRONTONASAL DYSPLASIA 2 (OMIM:613451)
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..Furlong syndrome (C538192)
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..Genoa syndrome (C537684)
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..Hordnes Engebretsen Knudtson syndrome (C536067)
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..Hunter-McAlpine syndrome (C536072)
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..Iida Kannari syndrome (C536284)
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..Jackson-Weiss syndrome (C537559)
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..Kleeblattschaedel syndrome (C536884)
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..Lowry Maclean syndrome (C537037)
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..Mehta Lewis Patton syndrome (C536147)
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..Muenke Syndrome (C537369)
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..Oculopalatoskeletal syndrome (C537738)
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..Opitz trigonocephaly syndrome (C537418)
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..Pfeiffer Tietze Welte syndrome (C537891)
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..Piepkorn Karp Hickok syndrome (C535774)
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..Plagiocephaly and X-linked mental retardation (C537512)
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..Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia (C564881)
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..Scaphocephaly, Maxillary Retrusion, And Mental Retardation (C566511)
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..Shprintzen Golberg craniosynostosis (C537328)
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..Skeletal dysplasia, San Diego type (C536670)
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..Spondyloepiphyseal Dysplasia With Coronal Craniosynostosis, Cataracts, Cleft Palate, And Mental Retardation (C566515)
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..Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet (C564759)
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..TRIGONOCEPHALY 1 (OMIM:190440)
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..Trigonocephaly, Nonsyndromic (C562951)
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..Warman Mulliken Hayward syndrome (C536684)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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