Inborn glycerol kinase deficiency
- Synonyms
- Deficiency of glycerol kinase; GK deficiency; GK1 deficiency; Glycerol Kinase Deficiency; Hyperglycerolemia
Summary
Excerpted from the GeneReview:- Full text of GeneReview (by section):
- Summary
- GeneReview Scope
- Diagnosis
- Clinical Characteristics
- Genetically Related Disorders
- Differential Diagnosis
- Management
- Genetic Counseling
- Resources
- Molecular Genetics
- References
- Chapter Notes
- Authors:
- John C Achermann
- Eric J Vilain
- view full author information
Available tests
Check Related conditions for additional relevant tests.
Clinical tests (31 available)
Biochemical Genetics Tests
Clinical features
Help- Abnormality of head or neck
- Downturned corners of mouth
Downturned corners of mouth
- MedGen UID: 356471
- Concept ID: C1866195
- Finding: Anatomical Abnormality
Abnormality of head or neck
- Downturned corners of mouth
- Abnormality of metabolism/homeostasis
- Hypertriglyceridemia
Hypertriglyceridemia
- MedGen UID: 167238
- Concept ID: C0813230
- Finding: Finding
Abnormality of metabolism/homeostasis
- Hypoglycemia
Hypoglycemia
- MedGen UID: 6979
- Concept ID: C0020615
- Finding: Disease or Syndrome
Abnormality of metabolism/homeostasis
- Inborn glycerol kinase deficiency
Inborn glycerol kinase deficiency
- MedGen UID: 82803
- Concept ID: C0268418
- Finding: Disease or Syndrome
Abnormality of metabolism/homeostasis
- Increased circulating lactate concentration
Increased circulating lactate concentration
- MedGen UID: 332209
- Concept ID: C1836440
- Finding: Finding
Abnormality of metabolism/homeostasis
- Ketoacidosis
Ketoacidosis
- MedGen UID: 67434
- Concept ID: C0220982
- Finding: Disease or Syndrome
Abnormality of metabolism/homeostasis
- Metabolic acidosis
Metabolic acidosis
- MedGen UID: 65117
- Concept ID: C0220981
- Finding: Pathologic Function
Abnormality of metabolism/homeostasis
- Reduced glycerol kinase activity in cultured fibroblasts
Reduced glycerol kinase activity in cultured fibroblasts
- MedGen UID: 1050791
- Concept ID: CN375682
- Finding: Finding
Abnormality of metabolism/homeostasis
- Hypertriglyceridemia
- Abnormality of the digestive system
- Episodic vomiting
Episodic vomiting
- MedGen UID: 333228
- Concept ID: C1838993
- Finding: Finding
Abnormality of the digestive system
- Nausea
Nausea
- MedGen UID: 10196
- Concept ID: C0027497
- Finding: Sign or Symptom
Abnormality of the digestive system
- Vomiting
Vomiting
- MedGen UID: 12124
- Concept ID: C0042963
- Finding: Sign or Symptom
Abnormality of the digestive system
- Episodic vomiting
- Abnormality of the endocrine system
- Adrenal insufficiency
Adrenal insufficiency
- MedGen UID: 1351
- Concept ID: C0001623
- Finding: Disease or Syndrome
Abnormality of the endocrine system
- Adrenocortical hypoplasia
Adrenocortical hypoplasia
- MedGen UID: 870278
- Concept ID: C4024719
- Finding: Anatomical Abnormality
Abnormality of the endocrine system
- Adrenal insufficiency
- Abnormality of the eye
- Hypertelorism
Hypertelorism
- MedGen UID: 9373
- Concept ID: C0020534
- Finding: Finding
Abnormality of the eye
- Strabismus
Strabismus
- MedGen UID: 21337
- Concept ID: C0038379
- Finding: Disease or Syndrome
Abnormality of the eye
- Hypertelorism
- Abnormality of the genitourinary system
- Cryptorchidism
Cryptorchidism
- MedGen UID: 8192
- Concept ID: C0010417
- Finding: Congenital Abnormality
Abnormality of the genitourinary system
- Increased urinary glycerol
Increased urinary glycerol
- MedGen UID: 388667
- Concept ID: C2673558
- Finding: Finding
Abnormality of the genitourinary system
- Cryptorchidism
- Abnormality of the immune system
- Chronic pancreatitis
Chronic pancreatitis
- MedGen UID: 101753
- Concept ID: C0149521
- Finding: Disease or Syndrome
Abnormality of the immune system
- Chronic pancreatitis
- Abnormality of the musculoskeletal system
- Frontal bossing
Frontal bossing
- MedGen UID: 67453
- Concept ID: C0221354
- Finding: Congenital Abnormality
Abnormality of the musculoskeletal system
- Muscular dystrophy
Muscular dystrophy
- MedGen UID: 44527
- Concept ID: C0026850
- Finding: Disease or Syndrome
Abnormality of the musculoskeletal system
- Myopathy
Myopathy
- MedGen UID: 10135
- Concept ID: C0026848
- Finding: Disease or Syndrome
Abnormality of the musculoskeletal system
- Osteoporosis
Osteoporosis
- MedGen UID: 14535
- Concept ID: C0029456
- Finding: Disease or Syndrome
Abnormality of the musculoskeletal system
- Pathologic fracture
Pathologic fracture
- MedGen UID: 42095
- Concept ID: C0016663
- Finding: Pathologic Function
Abnormality of the musculoskeletal system
- Frontal bossing
- Abnormality of the nervous system
- Coma
Coma
- MedGen UID: 1054
- Concept ID: C0009421
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Global developmental delay
Global developmental delay
- MedGen UID: 107838
- Concept ID: C0557874
- Finding: Finding
Abnormality of the nervous system
- Intellectual disability
Intellectual disability
- MedGen UID: 811461
- Concept ID: C3714756
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Lethargy
Lethargy
- MedGen UID: 7310
- Concept ID: C0023380
- Finding: Sign or Symptom
Abnormality of the nervous system
- Loss of consciousness
Loss of consciousness
- MedGen UID: 52915
- Concept ID: C0041657
- Finding: Finding
Abnormality of the nervous system
- Seizure
Seizure
- MedGen UID: 20693
- Concept ID: C0036572
- Finding: Sign or Symptom
Abnormality of the nervous system
- Coma
- Constitutional symptom
- Myalgia
Myalgia
- MedGen UID: 68541
- Concept ID: C0231528
- Finding: Sign or Symptom
Constitutional symptom
- Myalgia
- Ear malformation
- Low-set ears
Low-set ears
- MedGen UID: 65980
- Concept ID: C0239234
- Finding: Congenital Abnormality
Ear malformation
- Low-set ears
- Growth abnormality
- Growth delay
Growth delay
- MedGen UID: 99124
- Concept ID: C0456070
- Finding: Pathologic Function
Growth abnormality
- Short stature
Short stature
- MedGen UID: 87607
- Concept ID: C0349588
- Finding: Finding
Growth abnormality
- Small for gestational age
Small for gestational age
- MedGen UID: 65920
- Concept ID: C0235991
- Finding: Finding
Growth abnormality
- Growth delay
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