X-linked dominant chondrodysplasia, Chassaing-Lacombe type (Q55782492)
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X-linked dominant chondrodysplasia Chassaing-Lacombe type is a rare genetic bone disorder characterized by chondrodysplasia, intrauterine growth retardation (IUGR), hydrocephaly and facial dysmorphism in the affected males
- CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA
- X-linked dominant chondrodysplasia-hydrocephaly-microphthalmia syndrome
- chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia
| Language | Label | Description | Also known as |
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| English | X-linked dominant chondrodysplasia, Chassaing-Lacombe type |
X-linked dominant chondrodysplasia Chassaing-Lacombe type is a rare genetic bone disorder characterized by chondrodysplasia, intrauterine growth retardation (IUGR), hydrocephaly and facial dysmorphism in the affected males |
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