Phenotypes for disease #02218 (NHS (Nance-Horan syndrome (NHS)), OMIM:302350)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000083941 congenital diaphragmatic hernia (HP:0000776 ), congenital cataract (HP:0000519) - - Familial, X-linked - - - - - Molka Kammoun 00106135
0000243036 (+) Abnormality of the lens,(+) Cataract / Cataracta congenita, no family history of cataract - - Unknown - - - - - Andreas Laner 00324493
0000304211 Developmental cataract, Abnormality of eye movement, Nystagmus, Hypospadias, Motor delay, Amblyopia, Global developmental delay 0y - Familial, X-linked dominant - - - - - Andreas Laner 00412197
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