progressive osseous heteroplasia
gene (20q13.2-q13.3), coding for guanine nucleotide-binding proteins. POH can, however, be distinguished clinically by the deep and progressive nature of the heterotopic bone formation.
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Summary
progressive osseous heteroplasia is a developmental defect during embryogenesis[1].
Key Facts
- progressive osseous heteroplasia's instance of is recorded as developmental defect during embryogenesis[2].
- progressive osseous heteroplasia's instance of is recorded as rare disease[3].
- progressive osseous heteroplasia's instance of is recorded as class of disease[4].
- progressive osseous heteroplasia is a type of heterotopic ossification[5].
- progressive osseous heteroplasia is a type of other dermis disorder[6].
- progressive osseous heteroplasia is a type of primary bone dysplasia with progressive ossification of skin, skeletal muscle, fascia, tendons and ligaments[7].
- progressive osseous heteroplasia is a type of other genetic dermis disorder[8].
- progressive osseous heteroplasia is a type of syndrome[9].
- progressive osseous heteroplasia is a type of autosomal dominant disease[10].
- progressive osseous heteroplasia's health specialty is recorded as dermatology[11].
- progressive osseous heteroplasia's genetic association is recorded as GNAS[12].
- progressive osseous heteroplasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111535[13].
- progressive osseous heteroplasia's exact match is recorded as http://identifiers.org/doid/DOID:0111535[14].