disease has feature syndromic intellectual disability syndromic disease epilepsy Wolf-Hirschhorn syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/5588 https://rarediseases.info.nih.gov/diseases/7896/wolf-hirschhorn-syndrome https://www.malacards.org/card/wolf_hirschhorn_syndrome microcephaly, IUGR, hypertelorism, ptosis, iris coloboma, hooked nose, external ear dysplasia, psychomotor retardation distal monosomy 4p chromosome 4p syndrome MONDO:0008684 DECIPHER:1 NANDO:2200962 UMLS:C1956097 Pitt-Rogers-Danks syndrome SCTID:718226002 MedDRA:10050361 Wolf-Hirschhorn syndrome (WHS) is a developmental disorder characterized by typical craniofacial features, prenatal and postnatal growth impairment, intellectual disability, severe delayed psychomotor development, seizures, and hypotonia. NCIT:C35528 WHS chromosome 4p16.3 deletion syndrome 4p syndrome MEDGEN:408255 GARD:0007896 icd11.foundation:1337401724 DOID:0050460 NORD:1859 MESH:D054877 4p deletion syndrome telomeric deletion 4p OMIM:194190 Wolf-Hirschhorn syndrome 4p- syndrome NANDO:1200683 distal deletion 4p Wolf-Hirschhorn syndrome, Isolated cases chromosome 4P16.3 deletion syndrome Wittwer syndrome Wolf syndrome Orphanet:280 Pitt syndrome multiple congenital anomalies/dysmorphic syndrome-intellectual disability obsolete syndromic genetic hearing loss obsolete chromosomal anomaly with cataract chromosome 4 short arm deletion