Human Gene Set: HP_CONGENITAL_STATIONARY_NIGHT_BLINDNESS


Standard name HP_CONGENITAL_STATIONARY_NIGHT_BLINDNESS
Systematic name M37104
Brief description Congenital stationary night blindness
Full description or abstract A nonprogressive (i.e., stationary) form of difficulties with night blindness with congenital onset. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0007642
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0007642
Filtered by similarity ? (show 1 similar ontology term(s) from the external resource)
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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