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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