has material basis in germline mutation in MPZ Charcot-Marie-Tooth disease type 1B https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/charcot_marie_tooth_disease_demyelinating_type_1b https://www.malacards.org/card/charcot_marie_tooth_disease_type_1b DOID:0110152 A sensorineural peripheral polyneuropathy affecting approximately 1 in 2,500 individuals, and is the most common inherited disorder of the peripheral nervous system. Autosomal dominant, autosomal recessive, and X-linked forms have been recognized. NCIT:C118782 MEDGEN:124377 HMSN1 HMSN1B OMIM:118200 Charcot Marie Tooth disease type 1B Charcot-Marie-Tooth disease type 1 caused by mutation in MPZ UMLS:C0270912 Charcot-Marie-Tooth disease, demyelinating, type 1B GARD:0001246 Orphanet:101082 HMSN 1B CMT 1B MPZ Charcot-Marie-Tooth disease type 1 CMT1B Charcot-Marie-Tooth disease, type 1B MONDO:0007307 HMSN IB icd11.foundation:1632280319 Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease type 1