ZFIN Human Disease: Aarskog syndrome

OBO ID: DOID:0111824

OBO ID: DOID:0111824

Term Name:	Aarskog syndrome	Search Ontology:
Synonyms:	faciodigitogenital syndrome
Definition:	A syndrome characterized by facial, limbs and genital anomalies, and a disproportionate acromelic short stature. https://ghr.nlm.nih.gov/condition/aarskog-scott-syndrome
References:	ORDO:915
Ontology:	Human Disease ( DOID:0111824 )

Relationships

is a type of:	syndrome syndrome Show first 5 Terms
has subtype:	autosomal dominant Aarskog syndrome X-linked Aarskog syndrome autosomal dominant Aarskog syndrome X-linked Aarskog syndrome Show first 5 Terms

OTHER Aarskog syndrome PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None