Rhizomelic chondrodysplasia punctata type 2 (Q95917): Difference between revisions
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Revision as of 11:45, 16 August 2026
This is a rare, developmental brain disorder characterised by systemic shortening of the proximal bones (i.e. rhizomelia), seizures, recurrent respiratory tract infections, and congenital cataracts. Type 2 (RCDP2) is associated with DHAPAT mutations.
| Language | Label | Description | Also known as |
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| default for all languages | ID_179969811 |
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| English | Rhizomelic chondrodysplasia punctata type 2 |
This is a rare, developmental brain disorder characterised by systemic shortening of the proximal bones (i.e. rhizomelia), seizures, recurrent respiratory tract infections, and congenital cataracts. Type 2 (RCDP2) is associated with DHAPAT mutations. |
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CID11:ID_179969811
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