C4020875 |
Mental and motor retardation
|
phenotype |
|
Pathologic Function
|
|
Abnormality of the nervous system
|
1020 |
C1843367 |
Poor school performance
|
phenotype |
|
Finding
|
|
Abnormality of the nervous system
|
984 |
C0557874 |
Global developmental delay
|
disease |
|
Mental or Behavioral Dysfunction
|
|
Abnormality of the nervous system
|
965 |
C1864897 |
Cognitive delay
|
phenotype |
|
Finding
|
|
Abnormality of the nervous system
|
965 |
C0025362 |
Mental Retardation
|
disease |
|
Mental or Behavioral Dysfunction
|
disease of mental health
|
Abnormality of the nervous system
|
947 |
C0423903 |
Low intelligence
|
phenotype |
|
Finding
|
|
Abnormality of the nervous system
|
946 |
C0917816 |
Mental deficiency
|
disease |
Behavior and Behavior Mechanisms; Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
|
Mental or Behavioral Dysfunction
|
|
Abnormality of the nervous system
|
946 |
C3714756 |
Intellectual Disability
|
group |
Behavior and Behavior Mechanisms; Mental Disorders; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
|
Mental or Behavioral Dysfunction
|
disease of mental health
|
Abnormality of the nervous system
|
946 |
C4020876 |
Dull intelligence
|
phenotype |
|
Finding
|
|
Abnormality of the nervous system
|
946 |
C0036572 |
Seizures
|
phenotype |
Nervous System Diseases; Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
disease of anatomical entity
|
Abnormality of the nervous system
|
759 |
C0349588 |
Short stature
|
phenotype |
|
Finding
|
|
Growth abnormality
|
749 |
C0014544 |
Epilepsy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the nervous system
|
735 |
C1858120 |
Generalized hypotonia
|
phenotype |
|
Finding
|
|
Abnormality of the musculature
|
632 |
C0424688 |
Small head
|
phenotype |
|
Finding
|
|
Abnormality of head or neck; Abnormality of the nervous system; Abnormality of the skeletal system
|
569 |
C0231246 |
Failure to gain weight
|
phenotype |
|
Finding
|
|
Growth abnormality
|
538 |
C2315100 |
Pediatric failure to thrive
|
disease |
|
Disease or Syndrome
|
|
Growth abnormality
|
528 |
C4531021 |
Undergrowth
|
phenotype |
|
Finding
|
|
|
528 |
C0950123 |
Genetic Diseases, Inborn
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Disease or Syndrome
|
genetic disease
|
|
505 |
C0028738 |
Nystagmus
|
disease |
Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the eye
|
485 |
C0026827 |
Muscle hypotonia
|
phenotype |
Nervous System Diseases; Pathological Conditions, Signs and Symptoms
|
Finding
|
|
Abnormality of the musculature
|
450 |
C0037932 |
Curvature of spine
|
phenotype |
Musculoskeletal Diseases
|
Finding
|
|
Abnormality of the skeletal system
|
406 |
C0018784 |
Sensorineural Hearing Loss (disorder)
|
disease |
Nervous System Diseases; Otorhinolaryngologic Diseases; Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
disease of anatomical entity
|
Abnormality of the ear
|
403 |
C0700208 |
Acquired scoliosis
|
phenotype |
|
Acquired Abnormality
|
|
Abnormality of the skeletal system
|
402 |
C0025990 |
Micrognathism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
|
Congenital Abnormality
|
|
Abnormality of head or neck; Abnormality of the skeletal system
|
396 |
C4024589 |
Aplasia/Hypoplasia of the mandible
|
phenotype |
|
Anatomical Abnormality
|
|
Abnormality of head or neck; Abnormality of the skeletal system
|
396 |