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

Official abbreviation NHS
Name Nance-Horan syndrome (NHS)
OMIM ID 302350
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene NHS
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00106135 - - - M no (Belgium) - - - - - NHS congenital diaphragmatic hernia (HP:0000776 ), congenital cataract (HP:0000519) NHS NHS 1 1 Molka Kammoun
00324493 173214 - - M ? Saudi Arabia - - - - - NHS (+) Abnormality of the lens,(+) Cataract / Cataracta congenita, no family history of cataract NHS NHS 1 1 Andreas Laner
00412197 199898 - - M no - - - - - - NHS Developmental cataract, Abnormality of eye movement, Nystagmus, Hypospadias, Motor delay, Amblyopia, Global developmental delay NHS NHS 1 1 Andreas Laner
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