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Glossary for Conductive hearing loss

Medical terms related to Conductive hearing loss or mentioned in this section include:

  • Acrofacial dysostosis, Nager type: A rare genetic disorder characterized by underdeveloped thumbs, forearm and cheekbones as well as ear defects.
  • Adenoiditis: Infection of the adenoids in the nasal-throat region
  • Body symptoms: Symptoms affecting the entire body features.
  • Brain symptoms: Symptoms affecting the brain
  • Branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct: A rare genetic disorder characterized by branchial defects, tear duct obstruction and pseudocleft of the upper lip.
  • Branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and: A rare genetic disorder characterized by branchial defects, tear duct obstruction and pseudocleft of upper lip.
  • Branchio-Oculo-Facial Syndrome: A rare genetic disorder characterized by branchial defects, lacrimal duct obstruction and pseudocleft of upper lip.
  • Buzzing in ears: The occurrence of buzzing in the ears
  • Cervicooculoacoustic syndrome: A rare genetic disorder characterized by ocular palsy, congenital perceptive deafness and fusion of the vertebrae in the neck.
  • Cholesteatoma: Uncommon middle ear condition
  • Chromosome 22q11 Deletion Spectrum: A rare chromosomal disorder where a small piece of genetic material is missing from chromosome 22 at the q11 location.
  • Cleft palate -- stapes fixation -- oligodontia: A very rare syndrome characterized by an opening in the roof of the mouth (cleft palate, the absence of six or more permanent teeth and hearing loss due to an inner ear abnormality (stapes fixation).
  • Common symptoms: The most common symptoms
  • Conductive deafness: Any hearing loss or impairment caused by a defect in part of the ear that conducts sound.
  • Cornelia de Lange syndrome 1: A very rare disorder involving delayed physical development and various malformations involving the head, face and limbs. Type 1 is more severe than type 2 though the range and severity of symptoms is variable.
  • Craniofacial dysostosis type 1: A rare genetic disorder characterized by premature joining of certain skull bones during development which has an impact on the shape of the head and face. Features include poor vision, hypoplasia of maxilla an impaired hearing.
  • Crouzon Syndrome: A condition which is characterized by craniofacial dysostosis
  • Deafness: Partial or complete hearing loss
  • Deletion 22q11: A rare chromosomal disorder where a small piece of genetic material is missing from chromosome 22 at the q11 location.
  • Dextrocardia-bronchiectasis-sinusitis: A genetic disorder characterized by sinusitis, bronchiectasis and situs inversus.
  • Down Syndrome: A chromosome syndrome causing physical effects and mental retardation.
  • Ear infection: Infection of the ear - may involve the middle and inner ear.
  • Ear symptoms: Symptoms affecting the ear or hearing
  • Ear wax: Buildup of wax (cerumen) inside the ear canal
  • Eccentrochondrodysplasia: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of certain enzymes needed to break it down.
  • Exostoses: Development of non-cancerous bony growths on bones. Pain can result depending on the size and location of the growth.
  • Face symptoms: Symptoms affecting the face
  • Facio-auriculo-radial dysplasia: A very rare syndrome characterized mainly by limb abnormalities, deafness and an abnormal heart rhythm.
  • Fara-Chlupackova syndrome: A rare syndrome characterized mainly by ear, face and neck abnormalities.
  • Glomus tympanicum: A rare, usually benign tumor found behind the ear drum. The tumor develops from glomus cells which are located along blood vessels involved in automatic body activities such as regulation of blood pressure and blood flow.
  • Goldenhar Syndrome: A congenital condition which affects the eyes, ears and vertebrae
  • Grief or loss: The normal emotional response that occurs to an external loss
  • Head symptoms: Symptoms affecting the head or brain
  • Hearing Impairment: Impaired ability to hear.
  • Hearing impairment: Impaired ability to hear.
  • Hearing loss: The loss of part or all of ones ability to hear
  • Hearing symptoms: Problems with the ear's hearing ability
  • Hearing voices: Hearing voices as a type of hallucination
  • Hypertelorism -- esophageal abnormalities -- hypospadias: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: one is inherited in a X-linked manner and the other is inherited in an autosomal dominant manner. Females with the X-linked form of the condition tend to have few symptoms and often only have wide set eyes.
  • Hypertelorism with esophageal abnormality and hypospadias: A congenital disorder characterized by distinctive facial features, genital abnormalities, esophageal defect and difficulty swallowing. Males are more severely affected than females.
  • Hypospadias -- hypertelorism: A congenital disorder characterized by distinctive facial features, genital abnormalities, esophageal defect and difficulty swallowing. Males are more severely affected than females.
  • Injury: Any damage inflicted in the body
  • LADD Syndrome: A very rare genetic disorder characterized by ear, teeth and tear duct abnormalities.
  • Lacrimoauriculodentodigital syndrome: A rare genetic disorder characterized by ear, teeth and tear duct abnormalities.
  • Lateral semicircular canal malformation, familial, with external and middle ear abnormalities: A rare familial syndrome characterized by various internal and external ear abnormalities.
  • Lop ears, Micrognathia and Conductive Hearing Loss: A very rare condition (described in only a few families) characterized by a small jaw, conductive hearing loss and abnormal ears.
  • Mastoiditis: Inflammation of a bone behind the ear
  • Melnick-Fraser syndrome: A rare genetic disorder characterized by hearing loss and kidney malformations. Type 1 involves a defect on the EYA1 gene on chromosome 8q13.3.
  • Mental retardation, X-linked, Reish type: A rare disorder characterized by mental retardation, brain anomalies, skeletal malformations, intestinal problems, eye and ear anomalies, cleft palate and kidney abnormalities. Some infants with the disorder die soon after birth due to breathing problems. The disorder is inherited in a X-linked manner which means that only males display the full range of symptoms whereas female carriers may have mild or no symptoms.
  • Middle ear infection: An infection which occurs in the middle ear
  • Mild conductive hearing loss: occurs when sound vibrations don't go from the air around the person to the moving ossicles
  • Mohr syndrome: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps and finger abnormalities.
  • Myhre Syndrome: A very rare inherited disorder characterized by retarded growth, mental retardation, bone abnormalities and distinctive facial features.
  • Nasopharyngeal carcinoma: A malignant cancer that occurs in the nasopharynx area which is the upper part of the throat. Often there are no symptoms until the cancer has metastasized to other parts of the body such as the neck.
  • Nerve symptoms: Symptoms affecting the nerves
  • Neurological symptoms: Any symptoms that are caused by neurological conditions
  • Oculoauriculovertebral (OAV) dysplasia: A congenital condition which affects the eyes, ears and vertebrae.
  • Opitz G Syndrome: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: one is inherited in a X-linked manner and the other is inherited in an autosomal dominant manner. Females with the X-linked form of the condition tend to have few symptoms and often only have wide set eyes.
  • Opitz G/BBB Syndrome: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: one is inherited in a X-linked manner and the other is inherited in an autosomal dominant manner. Females with the X-linked form of the condition tend to have few symptoms and often only have wide set eyes.
  • Opitz G/BBB Syndrome, Type II: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: Type I inherited in a X-linked manner and type II is inherited in an autosomal dominant manner.
  • Opitz G/BBB syndrome, Autosomal dominant: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: type I is inherited in a X-linked manner and type II is inherited in an autosomal dominant manner.
  • Opitz syndrome , X-linked: A congenital disorder characterized by distinctive facial features, genital abnormalities, esophageal defect and difficulty swallowing. Males are more severely affected than females.
  • Osteogenesis imperfecta: Weak bones ("brittle bone disease") and loose joints
  • Otitis externa: Infection of the outer ear canal
  • Oto-Palatal-digital syndrome: A very rare syndrome characterized a variety of abnormalities including skeletal anomalies, distinctive face and cleft palate. There are two types of the disorder (type 1 and 2) with type 2 being more severe.
  • Oto-Palato-Digital Syndrome:
  • Oto-Palato-digital syndrome type 1: A rare genetic disorder characterized by deafness, cleft palate, broad fingers and toes and short nails.
  • Oto-palato-digital syndrome, type 2: A rare genetic disorder characterized by head, face, mouth and bone abnormalities.
  • Otopalatodigital Syndrome Type I: A rare genetic disorder characterized by ear, palate, skull, face, finger, toe and other skeletal abnormalities. Type 1 is a milder form of the condition than type 2. Males tend to have more severe symptoms than females who may exhibit only facial anomalies.
  • Otopalatodigital Syndrome Type I and II: A rare genetic disorder characterized by ear, palate, skull, face, finger, toe and other skeletal abnormalities.
  • Otosclerosis: Genetic ear bone disorder
  • Paget's disease of bone: A chronic, slowly progressing bone disorder where the bone is destroyed rapidly and replaced by abnormal bone which is dense and fragile.
  • Pain: Any type of pain sensation symptoms.
  • Pierre Robin syndrome -- fetal chondrodysplasia: A very rare inherited disorder involving bone growth abnormalities, impaired hearing and a characteristic face.
  • Pierre-Robin syndrome with fetal chondrodysplasia: A very rare inherited disorder involving bone growth abnormalities, impaired hearing and a characteristic face.
  • Polychondritis: A serious, progressive, episodic condition characterized by inflammation and degeneration of cartilage in the body. The duration and severity of the episodes can vary.
  • Polydactyly cleft lip palate psychomotor retardation: A very rare syndrome described in a small inbred group of families and characterized by bifid toes, extra big fingers, cleft lip or palate and psychomotor retardation. There were various other symptoms that were variably present.
  • Richieri-Costa Pereira syndrome: A rare syndrome characterized mainly by the association of short stature, Pierre Robin sequence, cleft mandible, hand anomalies and clubfoot.
  • Sensations: Changes to sensations or the senses
  • Sensory symptoms: Symptoms affecting the sensory systems.
  • Shprintzen syndorme: An inherited syndrome of cardiac defects and craniofacial anomalies and various other abnormalities.
  • Skeletal and Cardiac Malformations with thrombocytopenia: A rare, newly described syndrome characterized by skeletal and heart abnormalities as well as a blood disorder.
  • Skeletal symptoms: Symptoms affecting the skeletal system such as the bones.
  • Skeleto cardiac syndrome with thrombocytopenia: A rare, newly described syndrome characterized by skeletal and heart abnormalities as well as a blood disorder.
  • Soto's Syndrome: A rare hereditary disorder characterized by excessive growth during the first few years of life as well as various other mental and physical anomalies.
  • Syndactyly, Cenani Lenz type: A rare birth defect syndrome characterized by various hand bone abnormalities.
  • Treacher-Collins Syndrome: A rare genetic disorder characterized by malar hypoplasia, down-slanting palpebral fissures, defect of lower eye lid and malformation of external ear.
  • Unusual facies, osteosarcoma and malformation syndrome: A rare syndrome characterized mainly by an unusual facial appearance, osteosarcoma, hearing problems and other variable abnormalities.
  • Velocardiofacial syndrome: A genetic disorder which can present with a wide range of phenotypic manifestations which has lead to a number of different names being assigned to the various presentations e.g. DiGeorge Syndrome and Cayler Anomaly Face Syndrome. There are nearly 200 different symptoms that can occur and the severity of the condition is also highly variable depending on the nature and severity of the symptoms that are present.
  • Wildervanck syndrome: A rare birth disorder involving hearing loss, fusion of vertebrae and eye movement abnormalities/
  • Zunich neuroectodermal syndrome: A very rare genetic syndrome characterized by a range of symptoms such as colobomas of the eye, heart defects, ichthyosiform dermatosis, mental retardation and ear defects.

Conditions listing medical symptoms: Conductive hearing loss:

The following list of conditions have 'Conductive hearing loss' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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Conditions listing medical complications: Conductive hearing loss:

The following list of medical conditions have 'Conductive hearing loss' or similar listed as a medical complication in our database.

 

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