Ring chromosome 9 syndrome

Orpha code: 96173OMIM code:

Definition

Ring chromosome 9 syndrome is an autosomal anomaly characterized by variable clinical features, most commonly including developmental delay, some degree of intellectual disability, facial dysmorphism, microcephaly, congenital heart anomalies, and variable genital, limb and skeletal anomalies.

Disease data
Classification

Malformation syndrome

Synonyms
Ring 9
Ring chromosome 9
Ring 9
Ring chromosome 9
ORPHA code
96173
OMIM code
-
ICD10 code
Q93.2
ICD11 code
-

No additional description.

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