LD2D
category
Phakomatoses or hamartoneoplastic syndromes
Exclusions
- Angio-osteohypertrophic syndrome
(LD26.60) - Ataxia-telangiectasia
(4A01.31) - Enchondromatosis
(4B4Z) - Maffucci syndrome
(4B4Y) - Proteus syndrome
(LD2C) - Rendu-Osler-Weber disease
(LA90.00) - Sturge-Weber syndrome
(LD23) - familial dysautonomia [Riley-Day]
(8C21.1)
7 subordinate codes
Nearby in Multiple developmental anomalies or syndromes
LD20Syndromes with central nervous system anomalies as a major featureLD21Syndromes with eye anomalies as a major featureLD22Syndromes with dental anomalies as a major featureLD23Syndromes with vascular anomalies as a major featureLD24Syndromes with skeletal anomalies as a major featureLD25Syndromes with face or limb anomalies as a major featureLD26Syndromes with limb anomalies as a major featureLD27Syndromes with skin or mucosal anomalies as a major feature