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Parent Node:
expandsyndromic craniosynostosis (MONDO:0015338)
..Starting node
..expandtrigonocephaly-broad thumbs syndrome ()

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..expandosteosclerosis-developmental delay-craniosynostosis syndrome ()
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..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:18064
Name:trigonocephaly-broad thumbs syndrome
Definition:Trigonocephaly-broad thumbs syndrome is characterized by neonatal trigonocephaly and multiple anomalies including craniosynostosis, shallow orbits, unusual nose, deviation of the terminal phalanges of fingers 1, 2, and 5, and broad toes with duplication of the terminal phalanx. It has been described in a mother and her son. It is transmitted as an autosomal dominant trait.
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Synonyms:Hunter Rudd Hoffmann syndrome; Hunter-Rudd-Hoffmann syndrome
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