Microphthalmia, Lenz type (Q94949): Difference between revisions
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Revision as of 10:30, 16 August 2026
Microphthalmia, Lenz type is a syndromic form of microphthalmia characterised by coloboma, microphthalmia and cataract, associated with skeletal and/or digital abnormalities affecting the clavicles and thumbs (clinodactily), intellectual deficit and growth disorders, microcephaly, detached ears, hollow palate and dental abnormalities, renal hypoplasia, cryptorchidism, and congenital cardiopathy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_678242327 |
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| English | Microphthalmia, Lenz type |
Microphthalmia, Lenz type is a syndromic form of microphthalmia characterised by coloboma, microphthalmia and cataract, associated with skeletal and/or digital abnormalities affecting the clavicles and thumbs (clinodactily), intellectual deficit and growth disorders, microcephaly, detached ears, hollow palate and dental abnormalities, renal hypoplasia, cryptorchidism, and congenital cardiopathy. |
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CID11:ID_678242327
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