Hijazi-reis syndrome

Preferred Label : Hijazi-reis syndrome;

Symbol : HIJRS;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Neurodevelopmental disorder with gait disturbance, dysmorphic facies, and behavioral abnormalities, X-linked; NEDGFAX;

Prefixed ID : #301094;

Details

Origin ID

301094;

UMLS CUI

C5774179;

Genes related to phenotype
- Transcription elongation factor a-like 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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