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Parent Node:
expandsyndromic craniosynostosis (MONDO:0015338)
..Starting node
..expandcraniosynostosis, Herrmann-Opitz type ()

       Child Nodes:



 Sister Nodes: 
..expandacrocephalopolydactyly ()
..expandacrocephalosyndactyly ()
..expandAntley-Bixler syndrome ()
..expandautosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome ()
..expandBaller-Gerold syndrome ()
..expandBeare-Stevenson cutis gyrata syndrome ()
..expandc syndrome ()
..expandcardiocranial syndrome, Pfeiffer type ()
..expandcloverleaf skull-asphyxiating thoracic dysplasia syndrome ()
..expandcloverleaf skull-multiple congenital anomalies syndrome ()
..expandcranioectodermal dysplasia ()
..expandcraniomicromelic syndrome ()
..expandcraniosynostosis and dental anomalies ()
..expandcraniosynostosis, Boston type ()
..expandcraniosynostosis, Herrmann-Opitz type ()
..expandcraniosynostosis, Philadelphia type ()
..expandcraniosynostosis-anal anomalies-porokeratosis syndrome ()
..expandcraniosynostosis-cataract syndrome ()
..expandcraniosynostosis-fibular aplasia syndrome ()
..expandcraniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome ()
..expandcraniosynostosis-intracranial calcifications syndrome ()
..expandcraniotelencephalic dysplasia ()
..expandCrouzon syndrome ()
..expandCrouzon syndrome-acanthosis nigricans syndrome ()
..expandcurry-Jones syndrome ()
..expandfamilial scaphocephaly syndrome ()
..expandholoprosencephaly-craniosynostosis syndrome ()
..expandHunter-McAlpine craniosynostosis ()
..expandlethal occipital encephalocele-skeletal dysplasia syndrome ()
..expandLowry-MacLean syndrome ()
..expandmetopic ridging-ptosis-facial dysmorphism syndrome ()
..expandMuenke syndrome ()
..expandosteosclerosis-developmental delay-craniosynostosis syndrome ()
..expandpseudoaminopterin syndrome ()
..expandscarf syndrome ()
..expandShprintzen-Goldberg syndrome ()
..expandSummitt syndrome ()
..expandtrigonocephaly-broad thumbs syndrome ()
..expandtrigonocephaly-short stature-developmental delay syndrome ()
..expandX-linked intellectual disability-plagiocephaly syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:16291
Name:craniosynostosis, Herrmann-Opitz type
Definition:Craniosynostosis, Herrmann-Opitz type is a rare bone development disorder characterized by intellectual disability, short stature, turribrachycephaly, facial dysmorphism (i.e. severe hypertelorism, hypoplasia of supraorbital ridges, abnormal ears, and micrognathia), bony defects of the occiput, and digital anomalies (incl. syndactyly, oligodactyly, and/or brachydactyly). Urethral atresia has also been reported. There have been no further descriptions in the literature since 1987.
Alternative IDs:
ParentIDs:
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Synonyms:Herrmann Opitz craniosynostosis
Slim Mappings:
Reference: MedGen:
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