ZFIN Human Disease: cerebrooculofacioskeletal syndrome

OBO ID: DOID:0080910

Term Name:	cerebrooculofacioskeletal syndrome		Search Ontology:
Synonyms:
Definition:	A Cockayne syndrome that is characterized by very severe prenatal developmental anomalies including microcephaly, congenital cataracts, severe mental retardation, facial dysmorphism, and arthrogryposis. https://www.ncbi.nlm.nih.gov/books/NBK1342/
References:	GARD:6027 OMIM:PS214150
Ontology:	Human Disease ( DOID:0080910 )

Relationships

is a type of:	Cockayne syndrome Cockayne syndrome Show first 5 Terms
has subtype:	cerebrooculofacioskeletal syndrome 1 cerebrooculofacioskeletal syndrome 2 cerebrooculofacioskeletal syndrome 3 cerebrooculofacioskeletal syndrome 4 cerebrooculofacioskeletal syndrome 1 cerebrooculofacioskeletal syndrome 2 cerebrooculofacioskeletal syndrome 3 cerebrooculofacioskeletal syndrome 4 Show first 5 Terms

OTHER cerebrooculofacioskeletal syndrome PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None