C84805Level 7
Lamellar Ichthyosis
**Semantic type:** Disease or Syndrome
**Definition:** A very rare, autosomal recessive inherited skin disorder present at birth. It is characterized by the presence of a transparent membrane encasing the newborn. This membrane sheds in about two weeks after birth to reveal generalized scaling and skin erythema.
GET
/api/v1/systems/nci_thesaurus/nodes/C84805Hierarchy Explorer
Hierarchy Explorer
Cross-system equivalences0
No cross-system equivalences mapped for this node.