Autosomal dominant hereditary disorder	Congenital anomaly of limb	Developmental hereditary disorder	Disorder of embryonic structure
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Mullerian duct and limb anomalies syndrome (disorder)
	Mullerian duct and limb anomalies syndrome
	Syndrome with the association of mullerian duct and distal limb anomalies. It has been described in five individuals from one family. Females presented with anomalies ranging from a vaginal septum to complete duplication of uterus and vagina, and males presented with micropenis. The limb anomalies varied from postaxial polydactyly to severe upper limb hypoplasia with split hand. The mode of transmission is autosomal dominant.
	syndroom van anomalie van gang van Müller en extremiteit
	syndroom van anomalie van buis van Müller en extremiteit syndroom van anomalie van ductus paramesonephricus en extremiteit

Id	716111003
Status	Primitive

Associated morphology	Morphologically abnormal structure
Finding site	Limb structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Morphologically abnormal structure
Finding site	Structure of paramesonephric duct
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8
Correlation	SNOMED CT source code to target map code correlation not specified