HPCA:Ensemblv90

hippocalcin
OMIM: 142622, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Red HPCA in Cerebral Palsy Level 2: Neurology and neurodevelopmental disorders Version 1.405	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Expert list Phenotypes Dystonia 2, torsion, autosomal recessive, MIM#224500
Green HPCA in Mendeliome Version 1.3802	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Dystonia 2, torsion, autosomal recessive, MIM# 224500 MONDO:0009141
Green HPCA in Dystonia - isolated/combined Level 2: Neurology and neurodevelopmental disorders Version 1.42 Component of the following Super Panels: Dystonia_Superpanel Progressive Neurological Conditions Tremors_Superpanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Dystonia 2, torsion, autosomal recessive, 224500 MONDO:0009141 childhood-onset generalized dystonia adolescence-onset segmental dystonia generalized dystonia with additional neurological features
Red HPCA in Cerebral Palsy Level 2: Neurology and neurodevelopmental disorders Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Expert Review Red Phenotypes Dystonia 2, torsion, autosomal recessive, MIM#224500
Green HPCA in Dystonia - isolated/combined Level 2: Neurology and neurodevelopmental disorders Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Royal Melbourne Hospital Expert Review Green Phenotypes Dystonia 2, torsion, autosomal recessive, 224500 MONDO:0009141 childhood-onset generalized dystonia adolescence-onset segmental dystonia generalized dystonia with additional neurological features