Disease #01757 (DMC (Dyggve-Melchior-Clausen disease), OMIM:223800)
| Official abbreviation |
DMC |
| Name |
Dyggve-Melchior-Clausen disease |
| OMIM ID |
223800 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
DYM |
| Associated tissues |
- |
| Disease features |
height below 2SD, OFC below 3rd percentile, coarse facies, short neck, short trunk, brachydactyly, barrel chest/pectus carinatum, abdominal distension, lumbar lordosis, restricted major joint mobility, waddling gait, intellectual disability/global developmental delay, no odontoid hypoplasia, platyspondyly, double hump vertebral bodies, short and broad ilia with basilar hypoplasia, lacy iliac crests, rhizomelic upper/lower limbs, irregularities epiphyses, irregularities metaphysis, shortened metacarpals, shortened phalanges, carpal bone irregularities, genua valga |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2023-01-31 21:02:09 +01:00 (CET) |
Individuals
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