Autosomal ichthyosis syndrome with prominent neurologics signs

Synonym:	Autosomal ichthyosis syndrome with prominent neurologic signs

Orphanet:	ORPHA281238

Term Hierarchy

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

Autosomal ichthyosis syndrome with prominent neurologics signs
Autosomal ichthyosis syndrome with prominent neurologics signs

MedGen
Orofaciodigital syndrome type 14
Orofaciodigital syndrome type 14

MedGen
Eif3a eukaryotic translation initiation factor 3, subunit A [Rattus norvegicus]
Eif3a eukaryotic translation initiation factor 3, subunit A [Rattus norvegicus]
Gene ID:292148

Gene
GRM7 glutamate metabotropic receptor 7 [Homo sapiens]
GRM7 glutamate metabotropic receptor 7 [Homo sapiens]
Gene ID:2917

Gene
Leber congenital amaurosis 19
Leber congenital amaurosis 19

MedGen

Your browsing activity is empty.

Activity recording is turned off.