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Hypertyrosinemia, Richner-Hanhart type

disorder
SNOMED 4887000CUI C0268487

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Epidermal hyperkeratosis
Very frequent (80-99%)HP:0000962
Keratoderma
Very frequent (80-99%)HP:0000982
Mental deficiency
Very frequent (80-99%)HP:0001249
Scarring or clouding of the cornea of the eye
Very frequent (80-99%)HP:0007957
Amino acid levels abnormal
Frequent (30-79%)HP:0004337
Behavioral symptoms
Frequent (30-79%)HP:0000708
Involuntary, rapid, rhythmic eye movements
Frequent (30-79%)HP:0000639
Photophobia
Frequent (30-79%)HP:0000613
Sweating
Frequent (30-79%)HP:0000975
Abnormal nail morphology
Occasional (5-29%)HP:0001597
Abnormal vocalization
Occasional (5-29%)HP:0002167
Ataxia
Occasional (5-29%)HP:0001251
Decreased size of cranium
Occasional (5-29%)HP:0000252
Epilepsy
Occasional (5-29%)HP:0001250
Tremor
Occasional (5-29%)HP:0001337
Visual loss
Occasional (5-29%)HP:0000572
Zygomatic flattening
Occasional (5-29%)HP:0000272
4-Hydroxyphenylpyruvic aciduria
HP:0003161
Dendritic corneal epithelial ulcer
HP:0007812
Dermatopathy
HP:0000951
Elevated urine N-acetyltyrosine level
HP:6000479
Hypertyrosinemia
HP:0003231
Very poor growth
HP:0001510

Quick Facts

SNOMED CT
4887000
UMLS CUI
C0268487
Fully Specified Name
Hypertyrosinemia, Richner-Hanhart type (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
23
Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.