Naegeli–Franceschetti–Jadassohn syndrome
Naegeli-Franceschetti-Jadassohn (NFJ) syndrome is a rare ectodermal dysplasia that affects the skin, sweat glands, nails, and teeth
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Naegeli–Franceschetti–Jadassohn syndrome
Summary
Naegeli–Franceschetti–Jadassohn syndrome is a developmental defect during embryogenesis[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- Naegeli–Franceschetti–Jadassohn syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Naegeli–Franceschetti–Jadassohn syndrome's instance of is recorded as rare disease[4].
- Naegeli–Franceschetti–Jadassohn syndrome's instance of is recorded as class of disease[5].
- Naegeli–Franceschetti–Jadassohn syndrome is a type of ectodermal dysplasia[6].
- Naegeli–Franceschetti–Jadassohn syndrome is a type of autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature[7].
- Naegeli–Franceschetti–Jadassohn syndrome is a type of hyperpigmentation of the skin[8].
- Naegeli–Franceschetti–Jadassohn syndrome is a type of autosomal dominant disease[9].
- Naegeli–Franceschetti–Jadassohn syndrome is a type of disease[10].
- Naegeli–Franceschetti–Jadassohn syndrome's genetic association is recorded as KRT14[11].
- Naegeli–Franceschetti–Jadassohn syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_69087[12].
- Naegeli–Franceschetti–Jadassohn syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111528[13].
- Naegeli–Franceschetti–Jadassohn syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111528[14].
Why It Matters
Naegeli–Franceschetti–Jadassohn syndrome is known by 7 alternative names across languages and contexts.[2]