|
miliaria crystallina
|
DOID_0070321 |
[A miliaria that is characterized by clear, superficial, noninflammed, subcorneal vesicles that easily rupture when rubbed and is located_in the stratum corneum.] |
|
carbohydrate metabolic disorder
|
DOID_2978 |
[An inherited metabolic disorder that affect the catabolism and anabolism of carbohydrates.] |
|
childhood hepatocellular carcinoma
|
DOID_0070322 |
[A hepatocellular carcinoma that occurs in children and is characterized by a distinct etiological predisposition, biological behavior, and lower frequency of cirrhosis as compared to adult hepatocellular carcinoma.] |
|
bent bone dysplasia syndrome 1
|
DOID_0060992 |
[A bone remodeling disease characterized by poor mineralization of the calvarium, craniosynostosis, dysmorphic facial features, prenatal teeth, hypoplastic pubis and clavicles, osteopenia, and bent long bones that has_material_basis_in heterozygous mutation in the FGFR2 gene on chromosome 10q26.] |
|
dizziness
|
SYMP_0000610 |
[A balance symptom that is characterized by a sensation of unsteadiness accompanied by a feeling of movement within the head.] |
|
mitochondrial DNA depletion syndrome
|
DOID_0070329 |
[A mitochondrial metabolism disease that is characterized by significant reduction in mitochondrial DNA in affected tissues, resulting in impaired mtDNA-encoded protein synthesis and energy production in the affected tissues and organs.] |
|
main group molecular entity
|
CHEBI_33579 |
|
|
molecular entity
|
CHEBI_23367 |
|
|
exanthema
|
SYMP_0000629 |
[A rash characterized by a widespread skin eruption usually occurring in children that is a symptom of a more general disease.] |
|
rash
|
SYMP_0000487 |
[A skin and integumentary tissue symptom that is characterized by an eruption on the body typically with little or no elevation above the surface.] |
|
disturbed vision
|
SYMP_0000627 |
|
|
carboxylic acid
|
CHEBI_33575 |
|
|
organic acid
|
CHEBI_64709 |
|
|
carbon oxoacid
|
CHEBI_35605 |
|
|
conscious disturbance
|
SYMP_0000625 |
[An alteration of consciousness that is characterized by a disturbance in sentience (the ability to experience feelings and sensations) or awareness of one's internal and external existence, i.e. inhibited or absent self-awareness.] |
|
acute mesenteric lymphadenitis
|
SYMP_0000622 |
|
|
acute renal failure
|
SYMP_0000623 |
[A renal failure that is characterized by a severe and sudden onset of renal failure.] |
|
renal failure
|
SYMP_0000731 |
[A urinary system symptom that is characterized by a loss of excretory function in one or both kidneys, leading to retention of nitrogenous waste products from the blood.] |
|
multiple mitochondrial dysfunctions syndrome
|
DOID_0070330 |
[A mitochondrial metabolism disease that is characterized by reduced function of more than one stage of energy production resulting from mitochondria impairment.] |
|
mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition
|
DOID_0060982 |
[A mosaic variegated aneuploidy syndrome that is characterized by increased susceptibility to benign and malignant neoplasms beginning in early childhood that has_material_basis_in compound heterozygous mutation in the MAD1L1 gene on chromosome 7p22.] |