Autosomal dominant keratitis-ichthyosis-hearing loss syndrome
- Synonyms
- KID syndrome, autosomal dominant; Keratitis-ichthyosis-deafness syndrome, autosomal dominant; Senter syndrome
Summary
Available tests
Clinical tests (58 available)
Clinical features
Help- Abnormality of head or neck
- Furrowed tongue
Furrowed tongue
- MedGen UID: 21583
- Concept ID: C0040412
- Finding: Anatomical Abnormality
Abnormality of head or neck
- Microdontia
Microdontia
- MedGen UID: 66008
- Concept ID: C0240340
- Finding: Congenital Abnormality
Abnormality of head or neck
- Oral mucosa leukoplakia
Oral mucosa leukoplakia
- MedGen UID: 9738
- Concept ID: C0023532
- Finding: Neoplastic Process
Abnormality of head or neck
- Sparse eyebrow
Sparse eyebrow
- MedGen UID: 371332
- Concept ID: C1832446
- Finding: Finding
Abnormality of head or neck
- Furrowed tongue
- Abnormality of limbs
- Knee flexion contracture
Knee flexion contracture
- MedGen UID: 98042
- Concept ID: C0409355
- Finding: Finding
Abnormality of limbs
- Pes cavus
Pes cavus
- MedGen UID: 675590
- Concept ID: C0728829
- Finding: Congenital Abnormality
Abnormality of limbs
- Knee flexion contracture
- Abnormality of the eye
- Blindness
Blindness
- MedGen UID: 99138
- Concept ID: C0456909
- Finding: Disease or Syndrome
Abnormality of the eye
- Corneal ulceration
Corneal ulceration
- MedGen UID: 40486
- Concept ID: C0010043
- Finding: Disease or Syndrome
Abnormality of the eye
- Recurrent corneal erosions
Recurrent corneal erosions
- MedGen UID: 56353
- Concept ID: C0155119
- Finding: Disease or Syndrome
Abnormality of the eye
- Blindness
- Abnormality of the immune system
- Keratitis
Keratitis
- MedGen UID: 44013
- Concept ID: C0022568
- Finding: Disease or Syndrome
Abnormality of the immune system
- Keratoconjunctivitis sicca
Keratoconjunctivitis sicca
- MedGen UID: 9620
- Concept ID: C0022575
- Finding: Disease or Syndrome
Abnormality of the immune system
- Recurrent bacterial skin infections
Recurrent bacterial skin infections
- MedGen UID: 322727
- Concept ID: C1835686
- Finding: Finding
Abnormality of the immune system
- Keratitis
- Abnormality of the integument
- Absent axillary hair
Absent axillary hair
- MedGen UID: 347869
- Concept ID: C1859392
- Finding: Finding
Abnormality of the integument
- Absent pubic hair
Absent pubic hair
- MedGen UID: 349155
- Concept ID: C1859391
- Finding: Finding
Abnormality of the integument
- Hyperkeratosis
Hyperkeratosis
- MedGen UID: 209030
- Concept ID: C0870082
- Finding: Disease or Syndrome
Abnormality of the integument
- Hypohidrosis
Hypohidrosis
- MedGen UID: 43796
- Concept ID: C0020620
- Finding: Disease or Syndrome
Abnormality of the integument
- Ichthyosis
Ichthyosis
- MedGen UID: 7002
- Concept ID: C0020757
- Finding: Disease or Syndrome
Abnormality of the integument
- Nail dysplasia
Nail dysplasia
- MedGen UID: 331737
- Concept ID: C1834405
- Finding: Congenital Abnormality
Abnormality of the integument
- Nail dystrophy
Nail dystrophy
- MedGen UID: 66368
- Concept ID: C0221260
- Finding: Disease or Syndrome
Abnormality of the integument
- Sparse eyelashes
Sparse eyelashes
- MedGen UID: 375151
- Concept ID: C1843300
- Finding: Finding
Abnormality of the integument
- Trichiasis
Trichiasis
- MedGen UID: 66367
- Concept ID: C0221259
- Finding: Disease or Syndrome
Abnormality of the integument
- Absent axillary hair
- Abnormality of the musculoskeletal system
- Corneal scarring
Corneal scarring
- MedGen UID: 83899
- Concept ID: C0349702
- Finding: Finding
Abnormality of the musculoskeletal system
- Elbow flexion contracture
Elbow flexion contracture
- MedGen UID: 98367
- Concept ID: C0409338
- Finding: Acquired Abnormality
Abnormality of the musculoskeletal system
- Corneal scarring
- Abnormality of the nervous system
- Photophobia
Photophobia
- MedGen UID: 43220
- Concept ID: C0085636
- Finding: Sign or Symptom
Abnormality of the nervous system
- Photophobia
- Ear malformation
- Sensorineural hearing loss disorder
Sensorineural hearing loss disorder
- MedGen UID: 9164
- Concept ID: C0018784
- Finding: Disease or Syndrome
Ear malformation
- Sensorineural hearing loss disorder
- Neoplasm
- Squamous cell carcinoma
Squamous cell carcinoma
- MedGen UID: 2874
- Concept ID: C0007137
- Finding: Neoplastic Process
Neoplasm
- Squamous cell carcinoma
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