| syndroom van faciale dysmorfie, hypertrichose, epilepsie, verstandelijke beperking en/of ontwikkelingsachterstand en gingivale overgroei (aandoening) | | syndroom van faciale dysmorfie, hypertrichose, epilepsie, verstandelijke beperking en/of ontwikkelingsachterstand en gingivale overgroei | | FHEIG-syndroom
syndroom van faciale dysmorfie, hypertrichose, epilepsie, verstandelijke handicap en/of ontwikkelingsachterstand en overgroei van tandvlees
syndroom van faciale dysmorfie, hypertrichose, epilepsie, mentale retardatie en/of ontwikkelingsachterstand en overgroei van tandvlees
| | Facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth syndrome | | FHEIG (facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth) syndrome
FHEIG syndrome
| | A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by variable intellectual disability and/or developmental delay, epilepsy, generalized hypertrichosis, severe gingival overgrowth and visual impairment in some patients. Common craniofacial features include bitemporal narrowing, bushy and straight eyebrows, long eyelashes, low-set ears, deep/short philtrum, everted upper lip, prominent upper and lower vermilion, wide mouth, micrognathia, and retrognathia. |
| | Id | 1304114004 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | 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 |
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