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Nance-Horan syndrome | RareConnect | RareConnect.io

/hereditary disease

/disorder of development or morphogenesis

/Nance-Horan syndrome

Nance-Horan syndrome

Rare Disease

MONDO:0010545

Also Known As

Nance-Horan syndromenance-horan syndrome, X-linked dominantMesiodens cataract syndromeMesiodens-cataract syndromeNHScataract X-linked with Hutchinsonian teethcataract dental syndromecataract, X-linked, with Hutchinsonian teethcataract-dental syndrome

Definition

A syndrome characterized by the association in male patients of congenital cataracts with microcornea, dental anomalies and facial dysmorphism.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:302350 ↗

Orphanet

Orphanet:627 ↗

GARD

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