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Craniodigital syndrome and intellectual disability syndrome (disorder)
Craniodigital syndrome and intellectual disability syndrome
Scott Bryant Graham syndrome
Scott craniodigital syndrome
Syndrome with manifestations of syndactyly of the fingers and toes, characteristic facies (startled facial expression with a small pointed nose, micrognathia, long dark eyelashes and prominent eyebrows) and intellectual deficit. Less than 10 cases have been described in the literature so far. Abnormal dermatoglyphic patterns, growth retardation and brachycephaly have also been reported. Transmission appears to be autosomal or X-linked recessive.
craniodigitaal syndroom met verstandelijke beperking
craniodigitaal syndroom met verstandelijke handicap
syndroom van Scott-Bryant-Graham
craniodigitaal syndroom met mentale retardatie
craniodigitaal syndroom van Scott
Id763665007
StatusPrimitive
Associated morphologyCongenital abnormal fusion
Finding siteDigit structure
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyMorphologically abnormal structure
Finding siteFace structure
OccurrenceCongenital
Pathological processPathological developmental process
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ87.0
RuleTRUE
AdviceALWAYS Q87.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified