| Disease Browser
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Parent Node:
 craniosynostosis (MONDO:0015469) |
..Starting node
.. syndromic craniosynostosis ()
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Child Nodes:
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| ........acrocephalopolydactyly () |
| ........acrocephalosyndactyly () |
| ........Antley-Bixler syndrome () |
| ........autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome () |
| ........Baller-Gerold syndrome () |
| ........Beare-Stevenson cutis gyrata syndrome () |
| ........c syndrome () |
| ........cardiocranial syndrome, Pfeiffer type () |
| ........cloverleaf skull-asphyxiating thoracic dysplasia syndrome () |
| ........cloverleaf skull-multiple congenital anomalies syndrome () |
| ........cranioectodermal dysplasia () |
| ........craniomicromelic syndrome () |
| ........craniosynostosis and dental anomalies () |
| ........craniosynostosis, Boston type () |
| ........craniosynostosis, Herrmann-Opitz type () |
| ........craniosynostosis, Philadelphia type () |
| ........craniosynostosis-anal anomalies-porokeratosis syndrome () |
| ........craniosynostosis-cataract syndrome () |
| ........craniosynostosis-fibular aplasia syndrome () |
| ........craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome () |
| ........craniosynostosis-intracranial calcifications syndrome () |
| ........craniotelencephalic dysplasia () |
| ........Crouzon syndrome () |
| ........Crouzon syndrome-acanthosis nigricans syndrome () |
| ........curry-Jones syndrome () |
| ........familial scaphocephaly syndrome () |
| ........holoprosencephaly-craniosynostosis syndrome () |
| ........Hunter-McAlpine craniosynostosis () |
| ........lethal occipital encephalocele-skeletal dysplasia syndrome () |
| ........Lowry-MacLean syndrome () |
| ........metopic ridging-ptosis-facial dysmorphism syndrome () |
| ........Muenke syndrome () |
| ........osteosclerosis-developmental delay-craniosynostosis syndrome () |
| ........pseudoaminopterin syndrome () |
| ........scarf syndrome () |
| ........Shprintzen-Goldberg syndrome () |
| ........Summitt syndrome () |
| ........trigonocephaly-broad thumbs syndrome () |
| ........trigonocephaly-short stature-developmental delay syndrome () |
| ........X-linked intellectual disability-plagiocephaly syndrome () |
Sister Nodes: |
..craniosynostosis 4 ()
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..craniosynostosis 5, susceptibility to ()
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..craniosynostosis 7 ()
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..craniosynostosis alopecia brain defect ()
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..craniosynostosis arthrogryposis cleft palate ()
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..craniosynostosis autosomal dominant ()
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..craniosynostosis cleft lip palate arthrogryposis ()
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..craniosynostosis contractures cleft ()
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..craniosynostosis exostoses nevus epibulbar dermoid ()
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..craniosynostosis Fontaine type ()
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..craniosynostosis Maroteaux Fonfria type ()
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..craniosynostosis mental retardation heart defects ()
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..craniosynostosis syndrome, autosomal recessive ()
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..craniosynostosis with ectopia lentis ()
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..craniosynostosis with ocular abnormalities and hallucal defects ()
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..craniosynostosis, Adelaide type ()
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..glass-chapman-hockley syndrome ()
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..hordnes engebretsen knudtson syndrome ()
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..iida kannari syndrome ()
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..isolated craniosynostosis ()
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..mehta lewis patton syndrome ()
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..syndromic craniosynostosis ()
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MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
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