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Hyperleucine-isoleucinemia

MedGen UID:
82821
Concept ID:
C0268574
Disease or Syndrome
Synonym: Hyperleucine-Isoleucinemia
SNOMED CT: Hyperleucine-isoleucinemia (7046009)
 
Monarch Initiative: MONDO:0009385
OMIM®: 238340

Clinical features

From HPO
Failure to thrive
MedGen UID:
746019
Concept ID:
C2315100
Disease or Syndrome
Failure to thrive (FTT) refers to a child whose physical growth is substantially below the norm.
Sensorineural hearing loss disorder
MedGen UID:
9164
Concept ID:
C0018784
Disease or Syndrome
A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve.
Seizure
MedGen UID:
20693
Concept ID:
C0036572
Sign or Symptom
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain.
Intellectual disability
MedGen UID:
811461
Concept ID:
C3714756
Mental or Behavioral Dysfunction
Intellectual disability, previously referred to as mental retardation, is characterized by subnormal intellectual functioning that occurs during the developmental period. It is defined by an IQ score below 70.
Abnormality of metabolism/homeostasis
MedGen UID:
867398
Concept ID:
C4021768
Finding
Retinal degeneration
MedGen UID:
48432
Concept ID:
C0035304
Finding
A nonspecific term denoting degeneration of the retinal pigment epithelium and/or retinal photoreceptor cells.

Recent clinical studies

Diagnosis

Wang XL, Li CJ, Xing Y, Yang YH, Jia JP
J Inherit Metab Dis 2015 Sep;38(5):855-61. Epub 2015 Feb 5 doi: 10.1007/s10545-015-9814-z. PMID: 25653144

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