frontometaphyseal dysplasia

Summary

frontometaphyseal dysplasia is a hereditary disorder^[1].

Key Facts

• frontometaphyseal dysplasia's instance of is recorded as hereditary disorder^[2].
• frontometaphyseal dysplasia's instance of is recorded as rare disease^[3].
• frontometaphyseal dysplasia's instance of is recorded as class of disease^[4].
• frontometaphyseal dysplasia's subclass of is recorded as otopalatodigital syndrome spectrum disorder^[5].
• frontometaphyseal dysplasia's MeSH descriptor ID is recorded as C538064^[6].
• frontometaphyseal dysplasia's OMIM ID is recorded as 305620^[7].
• frontometaphyseal dysplasia's ICD-10 ID is recorded as Q78.5^[8].
• frontometaphyseal dysplasia's KEGG ID is recorded as H02227^[9].
• frontometaphyseal dysplasia's Disease Ontology ID is recorded as DOID:0111785^[10].
• frontometaphyseal dysplasia's Orphanet ID is recorded as 1826^[11].
• frontometaphyseal dysplasia's health specialty is recorded as medical genetics^[12].
• frontometaphyseal dysplasia's genetic association is recorded as FLNA^[13].
• frontometaphyseal dysplasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111785^[14].
• frontometaphyseal dysplasia's exact match is recorded as http://identifiers.org/doid/DOID:0111785^[15].
• frontometaphyseal dysplasia's UMLS CUI is recorded as C4281559^[16].
• frontometaphyseal dysplasia's UMLS CUI is recorded as C0265293^[17].
• frontometaphyseal dysplasia's GARD rare disease ID is recorded as 826^[18].
• frontometaphyseal dysplasia's Mondo ID is recorded as MONDO_0015942^[19].
• frontometaphyseal dysplasia's Genetics Home Reference Conditions ID is recorded as frontometaphyseal-dysplasia^[20].