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Focal Facial Dermal Dysplasia Type I (MONDO:0007627)

Focal facial dermal dysplasia type I (FFDD1), also known as Brauer syndrome, is a focal facial dysplasia (FFDD) characterized by congenital bitemporal cutis aplasia.

Overview

Category

integumentary system disorder

syndromic disease

Ontology ID

MONDO:0007627

Internal:8992

Synonyms

Brauer syndrome

FFDD type I

FFDD1

bitemporal aplasia cutis congenita

focal facial dermal dysplasia 1, Brauer type

focal facial dermal dysplasia type 1

FFDD, type 1

hereditary symmetrical aplastic nevi of temples

Mapped terms

GARD:0016524

MEDGEN:1718224

OMIM:136500

Orphanet:79133

UMLS:C5235196

Child terms

Unknown children.

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