has material basis in germline mutation in ELP1 skin disorder Riley-Day syndrome https://github.com/monarch-initiative/mondo/issues/5682 https://github.com/monarch-initiative/mondo/issues/6752 https://github.com/monarch-initiative/mondo/issues/6877 https://github.com/monarch-initiative/mondo/issues/9097 https://github.com/monarch-initiative/mondo/pull/2571/ https://www.malacards.org/card/neuropathy_hereditary_sensory_and_autonomic_type_iii GARD:0007581 hereditary sensory neuropathy type 3 MedDRA:10039179 ICD10CM:G90.1 NORD:1069 A congenital disorder caused by mutations in the IKBKAP gene. It is characterized by damage of the sympathetic and parasympathetic and sensory nervous system. HSAN 3 icd11.foundation:831377479 SCTID:29159009 Orphanet:1764 HSAN3 neuropathy, hereditary sensory and autonomic, type 3 hereditary sensory and autonomic neuropathy type III hereditary sensory and autonomic neuropathy 3 dysautonomia, familial DOID:11589 Dysautonomia, Familial HSAN III Riley Day syndrome OMIM:223900 neuropathy, hereditary sensory and autonomic, type III MONDO:0009131 MEDGEN:41678 UMLS:C0013364 hereditary sensory and autonomic neuropathy type 3 NCIT:C84706 familial dysautonomia MESH:D004402 Riley-Day syndrome HSN 3 obsolete neuro-ophthalmological disease primary orthostatic hypotension obsolete congenital alacrima dermis disorder neurocristopathy hereditary neurological disease