Kenny-Caffey syndrome, autosomal recessive

Preferred Label : Kenny-Caffey syndrome, autosomal recessive;

ICD-11 definition : Sanjad-Sakati syndrome is characterized by congenital hypoparathyroidism, growth retardation, intellectual deficit, seizures, and dysmorphic features including microcephaly, facial, ocular and dental abnormalities, and short hands and feet.;

ICD-11 inclusion : Sanjad-Sakati syndrome;

Details

Origin ID

740581484;

Automatic exact mappings (from CISMeF team)
- Autosomal recessive Kenny-Caffey syndrome [ORDO Disease]
- Kenny-Caffey syndrome, type 1 [MeSH Supplementary Concept]
- Kenny-caffey syndrome, type 1 [OMIM Phenotype]

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