| Preferred Name |
Lamellar Ichthyosis |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84805 |
| code |
C84805 |
| 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. |
| label |
Lamellar Ichthyosis |
| Preferred_Name |
Lamellar Ichthyosis |
| prefixIRI |
C84805 |
| prefLabel |
Lamellar Ichthyosis |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C0079154 |
| subClassOf |