OMOP Concept 3408034
Periorificial lentiginosis syndrome
Non-standardConditionNebraska Lexicon54411001Clinical Finding
Maps from
0
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Parent concepts
Broader concepts this one Is a kind of.
- Autosomal dominant hereditary disorder
- Congenital anomaly of intestinal tract
- Congenital hamartoma of skin
- Congenital melanosis
- Congenital pigmentary anomaly of skin
- Digestive system hereditary disorder
- Genetic disorder of skin pigmentation
- Hamartoma of intestine
- Hereditary disorder of nervous system
- Intestinal polyposis syndrome
- Lentiginosis
- Neuroectodermal dysplasia
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