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
C C- C1 C3 C5 C6 C7 CA CB CC CD CE CF CG CH CI CJ CK CL CM CN CO CP CQ CR CS CT CU CV CW CX CY CZ
CR3 CRA CRB CRC CRE CRI CRK CRL CRM CRO CRP CRR CRU CRY

craniofacial dysostosis

[autosomal dominant disorder characterized by acrocephaly, exophthalmos, hypertelorism, strabismus, parrot-beaked nose, and hypoplastic maxilla with relative mandibular prognathism. ( CSP )]
UMLS (CSP) C0010273
 
Congenital Abnormality
Disease or Syndrome
Relation/PAR: Dysostoses
Genetic Condition
Craniofacial Abnormalities
congenital oral/facial/cranial defect
Relation/CHD: Hallermann's Syndrome
Hypertelorism
Mandibulofacial Dysostosis

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