FGF4

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Amber FGF4 in Ciliopathies Level 2: Dysmorphic and congenital abnormality syndromes Version 1.76	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Short-rib thoracic dysplasia 22 without polydactyly, MIM# 621260
Amber FGF4 in Mendeliome Version 1.2833	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Short-rib thoracic dysplasia 22 without polydactyly, MIM# 621260
Amber FGF4 in Fetal anomalies Version 1.388	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Jeune Syndrome, FGF4-related, MONDO:0018770

3 panels