Human Phenotype Ontology
4041 terms(s) returned
Term Type: Class | Record: 4001 to 4041 of 4041 Records | Page: 81 of 81, First Previous Next Last | Show Records Per Page |
- Autonomic status epilepticus
- Autonomic-voluntary dissociation of facial movements
- Autophagia
- Autophagic vacuoles
- Autophony
- Autoscopy
- Autosomal dominant inheritance
- Autosomal dominant inheritance with maternal imprinting
- Autosomal dominant inheritance with paternal imprinting
- Autosomal recessive inheritance
- Autotopagnosia
- Avascular necrosis
- Avascular necrosis of the capital femoral epiphysis
- Avoidance of emotional intimacy
- Avoidance of stimuli associated with traumatic event
- Avulsion fracture
- Avulsion fractured epiphysis of femur
- Avulsion fractured humerus
- Avulsion fractured tibia
- Axenfeld anomaly
- Axial
- Axial dystonia
- Axial hypotonia
- Axial malrotation of the kidney
- Axial muscle atrophy
- Axial muscle stiffness
- Axial muscle weakness
- Axial myopia
- Axillary and groin hyperpigmentation and hypopigmentation
- Axillary apocrine gland hypoplasia
- Axillary epidermoid cyst
- Axillary freckling
- Axillary lymphadenopathy
- Axillary pterygium
- Axonal degeneration
- Axonal degeneration/regeneration
- Axonal loss
- Axonal regeneration
- Axonal spheroids
- Azoospermia
- Azotemia