Autosomal recessive hereditary disorder
Cerebellar ataxia
Congenital anomaly of retina
Congenital anomaly of skeletal bone
Congenital neurological disorder
Developmental hereditary disorder
Hereditary ataxia
Hereditary disorder of musculoskeletal system
Hereditary disorder of the visual system
Hereditary nephropathy
Renal dysplasia
Retinal pigment epithelial dystrophy
Skeletal dysplasia
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Saldino-Mainzer dysplasia (disorder)
Saldino-Mainzer dysplasia
Conorenal syndrome
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, skeletal dysplasia syndrome
Saldino-Mainzer-syndroom
conorenale dysplasie
conorenaal syndroom
Id
254092004
Status
Primitive
Associated morphology
Dysplasia
Finding site
Kidney structure
Occurrence
Congenital
Pathological process
Pathological developmental process
Associated morphology
Dysplasia
Finding site
Bone structure
Occurrence
Congenital
Pathological process
Pathological developmental process
Finding site
Cerebellar structure
Occurrence
Congenital
Associated morphology
Dystrophy
Finding site
Structure of retinal pigment epithelium
Occurrence
Congenital
Pathological process
Pathological developmental process
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
Target
Q61.4
Rule
TRUE
Advice
ALWAYS Q61.4
Correlation
SNOMED CT source code to target map code correlation not specified