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
P P- P0 P1 P2 P3 P4 P5 P6 P7 P8 P9 PA PB PC PD PE PF PG PH PI PK PL PM PN PO PP PQ PR PS PT PU PV PW PX PY
PD PD1 PDC PDD PDE PDF PDG PDI PDL PDP PDQ PDZ

5p Deletion Syndrome

[infantile syndrome characterized by a cat-like cry, failure to thrive, microcephaly, mental retardation, spastic quadriparesis, micro- and retrognathia, glossoptosis, bilateral epicanthus, hypertelorism, and tiny external genitalia; caused by a deletion of the short arm of chromosome 5. ( CSP )]
UMLS (NCI) C0010314
 
Congenital Abnormality
Disease or Syndrome
Relation/PAR: Abnormalities, Multiple
Chromosomal anomalies
syndrome
Chromosomal Disorders, Nervous System

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