Johnson–McMillin syndrome (Q16940647)

From Wikidata
Jump to navigation Jump to search
Johnson neuroectodermal syndrome is characterised by alopecia, anosmia or hyposmia, conductive deafness with malformed ears and microtia and/or atresia of the external auditory canal, and hypogonadotropic hypogonadism
  • Alopecia anosmia deafness hypogonadism syndrome
  • JOHNSON NEUROECTODERMAL SYNDROME
  • Alopecia-Anosmia-Deafness-Hypogonadism Syndrome
  • Aadh Syndrome
  • Johnson-Mcmillin Syndrome
  • Alopecia-anosmia-conductive hearing loss-hypogonadism syndrome
edit
Language Label Description Also known as
English
Johnson–McMillin syndrome
Johnson neuroectodermal syndrome is characterised by alopecia, anosmia or hyposmia, conductive deafness with malformed ears and microtia and/or atresia of the external auditory canal, and hypogonadotropic hypogonadism
  • Alopecia anosmia deafness hypogonadism syndrome
  • JOHNSON NEUROECTODERMAL SYNDROME
  • Alopecia-Anosmia-Deafness-Hypogonadism Syndrome
  • Aadh Syndrome
  • Johnson-Mcmillin Syndrome
  • Alopecia-anosmia-conductive hearing loss-hypogonadism syndrome

Statements

Identifiers

 
edit
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit