Hartsfield-Bixler-Demyer syndrome
human disease
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Hartsfield-Bixler-Demyer syndrome
Summary
Hartsfield-Bixler-Demyer syndrome is a head and neck disease[1].
Key Facts
- Hartsfield-Bixler-Demyer syndrome's instance of is recorded as head and neck disease[2].
- Hartsfield-Bixler-Demyer syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Hartsfield-Bixler-Demyer syndrome's instance of is recorded as rare disease[4].
- Hartsfield-Bixler-Demyer syndrome's instance of is recorded as class of disease[5].
- Hartsfield-Bixler-Demyer syndrome is a type of orofacial clefting syndrome[6].
- Hartsfield-Bixler-Demyer syndrome's genetic association is recorded as FGFR1[7].
- Hartsfield-Bixler-Demyer syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2117[8].