ZFIN Human Disease: orofaciodigital syndrome III

OBO ID: DOID:0060373

Term Name:	orofaciodigital syndrome III		Search Ontology:
Synonyms:	Sugarman syndrome
Definition:	An orofaciodigital syndrome that is characterized by dysmorphic facies and severe intellectual deficits, and has_material_basis_in autosomal recessive inheritance. https://rarediseases.info.nih.gov/diseases/10518/orofaciodigital-syndrome-3
References:	MESH:C557817 OMIM:258850 ORDO:2752 SNOMEDCT_US_2023_03_01:239030004 UMLS_CUI:C0406726
Ontology:	Human Disease ( DOID:0060373 )

Relationships

is a type of:	autosomal recessive disease orofaciodigital syndrome autosomal recessive disease orofaciodigital syndrome 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