ICD-11 classes
20 Developmental anomalies
Multiple developmental anomalies or syndromes
LD2H — Syndromic genetic deafness

ICD-11 LD2H — Syndromic genetic deafness

The diagnosis has no description.

The diagnosis includes nothing.

The diagnosis excludes nothing.

Diagnosis with code LD2H contains 10 clarifying diagnoses:

  1. LD2H.0 — Fraser syndrome
  2. LD2H.1 — Neuropathy with hearing impairment
  3. LD2H.2 — Progressive deafness with stapes fixation
  4. LD2H.3 — Waardenburg-Shah syndrome
  5. LD2H.4 — Usher syndrome
  6. LD44.N0 — CATCH 22 phenotype
  7. 5A00.02 — Pendred syndrome
  8. 5A05 — Generalised resistance to thyroid hormone
  9. LD2H.Y — Other specified syndromic genetic deafness
  10. LD2H.Z — Syndromic genetic deafness, unspecified

The diagnosis is included in 35 other classes.

  • CATCH 22 phenotype (LD44.N0)
  • Pendred syndrome (5A00.02)
  • Generalised resistance to thyroid hormone (5A05)
  • CHARGE syndrome (5A61.0)
  • Deafness - opticoacoustic nerve atrophy - dementia (5C53.2Y)
  • Ectodermal dysplasia - sensorineural deafness (LD27.0Y)
  • Hypoparathyroidism - deafness - renal disease (LD27.0Y)
  • Renal tubular acidosis - deafness (GB90.44)
  • Stapes ankylosis with broad thumbs and toes (LD2F.1Y)
  • Stickler syndrome (LD2F.1Y)
  • Thiamine-responsive megaloblastic anaemia syndrome (5C63.Y)
  • Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (8C73.Y)
  • Norrie disease (LD21.Y)
  • Fechtner syndrome (3B64.01)
  • Spondyloepiphyseal dysplasia, MacDermot type (LD24.3)
  • Oral-facial-digital syndrome type 1 (LD25.00)
  • Oral-facial-digital syndrome type 2 (LD25.00)
  • Oral-facial-digital syndrome type 3 (LD25.00)
  • Oral-facial-digital syndrome type 4 (LD25.00)
  • Oral-facial-digital syndrome type 6 (LD25.00)
  • Oral-facial-digital syndrome type 8 (LD25.00)
  • Otopalatodigital syndrome (LD25.1)
  • Kearns-Sayre syndrome (9C82.0)
  • Multiple synostoses syndrome (LD26.3)
  • Arthrogryposis-like hand anomaly - sensorineural deafness (LD26.4Y)
  • Cockayne syndrome (LD2B)
  • Keratitis – ichthyosis – deafness syndrome (LD27.2)
  • Connexin palmoplantar keratoderma with sensorineural deafness (EC20.30)
  • Deafness – enamel hypoplasia – nail defects (LD27.0Y)
  • Tietz hypomelanosis – deafness syndrome (EC23.2Y)
  • LEOPARD syndrome (LD2F.1Y)
  • Cutis verticis gyrata - retinitis pigmentosa - sensorineural deafness (LD27.Y)
  • Deafness, lymphoedema and leukaemia syndrome (BD93.0)
  • Long QT syndrome with hearing impairment (BC65.0)
  • Infantile Bartter syndrome with deafness (GB90.43)

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