UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
H H+ H1 HA HB HC HD HE HF HG HH HI HK HL HM HN HO HP HQ HR HS HT HU HV HX HY HZ
HEA HEB HEC HED HEE HEF HEI HEL HEM HEN HEP HER HES HET HEU HEV HEX HEY

HERED PROG MUSC DYSTRPHY

[general term for a group of inherited disorders which are characterized by progressive degeneration of skeletal muscles. ( CSP )]
UMLS (ICD9CM) C0026850
 
Congenital Abnormality
Disease or Syndrome
Relation/PAR: Genetic Condition
muscle disorder
Heredodegenerative Disorders, Nervous System
Muscular Disorders, Atrophic
Relation/CHD: Duchenne muscular dystrophy
myotonia atrophica
Duchenne muscular dystrophy
myotonia atrophica
facioscapulohumeral muscular dystrophy
Muscular Dystrophy, Emery-Dreifuss

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