Schöpf–Schulz–Passarge syndrome
SchC6pf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy
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Schöpf–Schulz–Passarge syndrome
Summary
Schöpf–Schulz–Passarge syndrome is a developmental defect during embryogenesis[1].
Key Facts
- Schöpf–Schulz–Passarge syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- Schöpf–Schulz–Passarge syndrome's instance of is recorded as rare disease[3].
- Schöpf–Schulz–Passarge syndrome's instance of is recorded as class of disease[4].
- Schöpf–Schulz–Passarge syndrome is a type of nonepidermolytic palmoplantar keratoderma[5].
- Schöpf–Schulz–Passarge syndrome is a type of autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature[6].
- Schöpf–Schulz–Passarge syndrome is a type of malformation syndrome with odontal and/or periodontal component[7].
- Schöpf–Schulz–Passarge syndrome is a type of polymalformative genetic syndrome with increased risk of developing cancer[8].
- Schöpf–Schulz–Passarge syndrome is a type of autosomal dominant disease[9].
- Schöpf–Schulz–Passarge syndrome is a type of ectodermal dysplasia[10].
- Schöpf–Schulz–Passarge syndrome's ICD-9-CM is recorded as 758.89[11].
- Schöpf–Schulz–Passarge syndrome's health specialty is recorded as medical genetics[12].
- Schöpf–Schulz–Passarge syndrome's genetic association is recorded as WNT10A[13].
- Schöpf–Schulz–Passarge syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_50944[14].
- Schöpf–Schulz–Passarge syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111647[15].
- Schöpf–Schulz–Passarge syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111647[16].