Disease #02218 (NHS (syndrome, Nance-Horan (NHS)), OMIM:302350)

Official abbreviation NHS
Name syndrome, Nance-Horan (NHS)
OMIM ID 302350
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene NHS
Associated tissues -
Disease features -
Remarks -


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00106135 - - - M no (Belgium) - - 0 - - NHS congenital diaphragmatic hernia (HP:0000776 ), congenital cataract (HP:0000519) NHS NHS 1 1 Molka Kammoun
00324493 173214 - - M ? Saudi Arabia - - 0 - - NHS (+) Abnormality of the lens,(+) Cataract / Cataracta congenita, no family history of cataract NHS NHS 1 1 Andreas Laner
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