Human Gene Set: HP_SCAPHOCEPHALY


Standard name HP_SCAPHOCEPHALY
Systematic name M38405
Brief description Scaphocephaly
Full description or abstract Scaphocephaly is a subtype of dolichocephaly where the anterior and posterior aspects of the cranial vault are pointed (boat-shaped). Scaphocephaly is caused by a precocious fusion of sagittal suture without other associated synostosis. [https://orcid.org/0000-0002-0736-9199, PMID:16156241, PMID:23960302]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0030799
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0030799
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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