terminal osseous dysplasia with pigmentary defects
Terminal osseous dysplasia-pigmentary defects syndrome is characterised by malformation of the hands and feet, pigmentary skin lesions on the face and scalp and digital fibromatosis
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terminal osseous dysplasia with pigmentary defects
Summary
terminal osseous dysplasia with pigmentary defects is a developmental defect during embryogenesis[1].
Key Facts
- terminal osseous dysplasia with pigmentary defects's instance of is recorded as developmental defect during embryogenesis[2].
- terminal osseous dysplasia with pigmentary defects's instance of is recorded as rare disease[3].
- terminal osseous dysplasia with pigmentary defects's instance of is recorded as class of disease[4].
- terminal osseous dysplasia with pigmentary defects is a type of hyperpigmentation[5].
- terminal osseous dysplasia with pigmentary defects is a type of osteochondrodysplasia[6].
- terminal osseous dysplasia with pigmentary defects is a type of hyperpigmentation of the skin[7].
- terminal osseous dysplasia with pigmentary defects is a type of acromelic dysplasia[8].
- terminal osseous dysplasia with pigmentary defects is a type of filamin-related bone disorder[9].
- terminal osseous dysplasia with pigmentary defects is a type of autosomal dominant disease[10].
- terminal osseous dysplasia with pigmentary defects is a type of syndrome[11].
- terminal osseous dysplasia with pigmentary defects's health specialty is recorded as dermatology[12].
- terminal osseous dysplasia with pigmentary defects's genetic association is recorded as FLNA[13].
- terminal osseous dysplasia with pigmentary defects's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_88630[14].
- terminal osseous dysplasia with pigmentary defects's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0112149[15].
- terminal osseous dysplasia with pigmentary defects's exact match is recorded as http://identifiers.org/doid/DOID:0112149[16].