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UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
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A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
E E0 E6 E7 EA EB EC ED EE EF EG EH EI EJ EK EL EM EN EO EP EQ ER ES ET EU EV EW EX EY
ENA ENC END ENE ENG ENH ENI ENK ENL ENM ENN ENO ENP ENR ENT ENU ENV ENZ

Encephalotrigeminal Syndrome

[A non-inherited congenital condition with vascular and neurological abnormalities. It is characterized by facial vascular nevi (PORT-WINE STAIN), and capillary angiomatosis of intracranial membranes (MENINGES; CHOROID). Neurological features include EPILEPSY; cognitive deficits; GLAUCOMA; and visual defects. ( MSH )]
UMLS (NCI) C0038505
 
Congenital Abnormality
Disease or Syndrome
Relation/PAR: Angiomatosis
angioma
Familiar Neoplastic Syndrome
Neurocutaneous Syndromes

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