World Of Taxonomy
D005489Level 6

Focal Dermal Hypoplasia

**Definition:** A genetic skin disease characterized by hypoplasia of the dermis, herniations of fat, and hand anomalies. It is found exclusively in females and transmitted as an X-linked dominant trait.

**Tree numbers:** - C05.116.099.370.380 - C16.131.077.350.424 - C16.131.831.350.424 - C16.320.322.186 - C16.320.850.250.424 - C17.800.804.350.424 - C17.800.827.250.424

**Synonyms:** - Dermal Hypoplasia, Focal - Goltz's Syndrome - Goltz Syndrome - Goltz Gorlin Syndrome - Goltz-Gorlin Syndrome

GET/api/v1/systems/mesh/nodes/D005489
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