ZFIN Human Disease: MLS syndrome

OBO ID: DOID:0111875

Term Name:	MLS syndrome		Search Ontology:
Synonyms:	linear skin defects with multiple congenital anomalies
Definition:	A syndrome characterized by linear skin defects and various other congenital anomalies. The classical diagnosis consisted of unilateral or bilateral microphthalmia and/or anophthalmia and linear skin defects but patients with a molecular diagnosis of MLS syndrome may not display eye abnormalities. (2)
References:	OMIM:PS309801
Ontology:	Human Disease ( DOID:0111875 )

Relationships

is a type of:	syndrome syndrome Show first 5 Terms
has subtype:	linear skin defects with multiple congenital anomalies 1 linear skin defects with multiple congenital anomalies 2 linear skin defects with multiple congenital anomalies 3 linear skin defects with multiple congenital anomalies 1 linear skin defects with multiple congenital anomalies 2 linear skin defects with multiple congenital anomalies 3 Show first 5 Terms

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Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None