disease arises from structure disease arises from alteration in structure 19q13.11 (Human) syndromic intellectual disability syndrome caused by partial chromosomal deletion chromosome 19q13.11 deletion syndrome https://github.com/monarch-initiative/mondo/issues/3664 https://github.com/monarch-initiative/mondo/issues/5588 https://rarediseases.info.nih.gov/diseases/10592/chromosome-19q1311-deletion-syndrome https://www.malacards.org/card/chromosome_19q1311_deletion_syndrome MONDO:0013090 The 19q13.11 microdeletion is characterized by several major features including pre and postnatal growth retardation, slender habitus, severe postnatal feeding difficulties, microcephaly, intellectual deficit with speech disturbance, hypospadias and ectodermal dysplasia presented by scalp aplasia, thin and sparse hair, eyebrows and eyelashes, thin and dry skin and dysplasic nails. Orphanet:217346 UMLS:C2751651 monosomy 19q13.11 MEDGEN:414432 Del(19)(q13.11) 19q13.11 microdeletion syndrome GARD:0010592 MESH:C567810 DOID:0060408 SCTID:719599008 multiple congenital anomalies/dysmorphic syndrome-intellectual disability partial deletion of the long arm of chromosome 19