Congenital macrocephaly	Developmental hereditary disorder	Intellectual disability	Short stature disorder	X-linked dominant hereditary disease
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X-linked intellectual disability Atkin type (disorder)
	Atkin Flaitz syndrome
	X-linked intellectual disability Atkin type
	Atkin-Flaitz syndrome has characteristics of moderate to severe intellectual deficit, short stature, macrocephaly, and characteristic facies. It has been described in 11 males and three females from three successive generations of the same family. The males also presented with postpubertal macroorchidism. Transmission is X-linked.
	X-gebonden verstandelijke beperking type Atkin
	syndroom van Atkin-Flaitz X-gebonden mentale retardatie type Atkin X-gebonden verstandelijke handicap type Atkin

Id	718577005
Status	Primitive

Associated morphology	Enlargement
Finding site	Head structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Interprets

Height / growth measure

Has interpretation	Above reference range
Interprets	Head circumference

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified