has material basis in germline mutation in ADNP congenital nervous system disorder ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder https://github.com/monarch-initiative/mondo/issues/5588 https://www.malacards.org/card/adnp_related_multiple_congenital_anomalies_intellectual_disability_autism_spectrum_disorder_2 https://www.malacards.org/card/helsmoortel_van_der_aa_syndrome GARD:0012931 MONDO:0014379 autosomal dominant intellectual disability 28 An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of ADNP on chromosome 20q13.13. Orphanet:404448 ADNP Syndrome Helsmoortel-Van der Aa syndrome ADNP syndrome DOID:0070058 intellectual disability, autosomal dominant 28 HVDAS OMIM:615873 SCTID:766824003 UMLS:C4014538 NORD:1965 mental retardation, autosomal dominant 28 ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder MEDGEN:862975 multiple congenital anomalies/dysmorphic syndrome-intellectual disability autosomal dominant syndromic intellectual disability