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(HPO:0000478) | Abnormality of the eye | Very frequent [Orphanet] | 126 / 7739 | |||
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(HPO:0000502) | Abnormality of the conjunctiva | 6 / 7739 | ||||
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(HPO:0001059) | Pterygium | 16 / 7739 | ||||
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(OMIM) | Wing-shaped conjunctival thickening in interpalpebral fissure | 1 / 7739 | ||||
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(HPO:0000481) | Abnormality of the cornea | Frequent [Orphanet] | 124 / 7739 | |||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |