teebi naguib al awadi syndrome

Preferred Label : teebi naguib al awadi syndrome;

MeSH synonym : profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence; al awadi teebi farag syndrome;

Details

Origin ID

C536949;

UMLS CUI

C2931374;

Automatic exact mappings (from CISMeF team)
- Autosomal recessive faciodigitogenital syndrome [ORDO Disease]
- Autosomal recessive faciodigitogenital syndrome (disorder) [SNOMED CT concept]
- Faciodigitogenital syndrome, autosomal recessive [OMIM Phenotype]
- Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) [SNOMED CT concept]
False automatic mappings
- Primary hypergonadotropic hypogonadism-partial alopecia syndrome [ORDO Disease]
MeSH term(s) associated for indexing
- osteochondrodysplasias [MeSH Descriptor]
Record concept(s)
- Teebi Naguib Al Awadi syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) [SNOMED CT concept]
- Primary hypergonadotropic hypogonadism-partial alopecia syndrome [ORDO Disease]

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