Syndromic genetic deafness

Child codes

• LD2H.0 – Fraser syndrome
• LD2H.1 – Neuropathy with hearing impairment
• LD2H.2 – Progressive deafness with stapes fixation
• LD2H.3 – Waardenburg-Shah syndrome
• LD2H.4 – Usher syndrome
• LD2H.Y – Other specified syndromic genetic deafness
• LD2H.Z – Syndromic genetic deafness, unspecified

Foundation children elsewhere

• 5A00.02 – Pendred syndrome
• 5A05 – Generalised resistance to thyroid hormone
• LD44.N0 – CATCH 22 phenotype

Sibling codes

• LD20 – Syndromes with central nervous system anomalies as a major feature
• LD21 – Syndromes with eye anomalies as a major feature
• LD22 – Syndromes with dental anomalies as a major feature
• LD23 – Syndromes with vascular anomalies as a major feature
• LD24 – Syndromes with skeletal anomalies as a major feature
• LD25 – Syndromes with face or limb anomalies as a major feature
• LD26 – Syndromes with limb anomalies as a major feature
• LD27 – Syndromes with skin or mucosal anomalies as a major feature
• LD28 – Syndromes with connective tissue involvement as a major feature
• LD29 – Syndromes with obesity as a major feature
• LD2A – Malformative disorders of sex development
• LD2B – Syndromes with premature ageing appearance as a major feature
• LD2C – Overgrowth syndromes
• LD2D – Phakomatoses or hamartoneoplastic syndromes
• LD2E – Syndromes with structural anomalies due to inborn errors of metabolism
• LD2F – Syndromes with multiple structural anomalies, without predominant body system involvement
• LD2G – Conjoined twins
• LD2Y – Other specified multiple developmental anomalies or syndromes
• LD2Z – Multiple developmental anomalies or syndromes, unspecified

Foundation entity

Syndromic genetic deafness – http://id.who.int/icd/entity/186534168