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🏥 Disease / Health Topic

Hereditary Retinal Dystrophy

0
Clinical Trials
0
Meta-Analyses
0
PubMed References
🏥 All Disease / Health Topic data fields for Hereditary Retinal Dystrophy
🏥 Names
Disease Name
Hereditary Retinal Dystrophy
Alias Names
Leber Congenital Amaurosis 4; Retinitis Pigmentosa 50; Retinitis Pigmentosa 77; Leber Congenital Amaurosis 8; Late-Adult Onset Retinitis Pigmentosa; Retinitis Pigmentosa 74; Retinitis Pigmentosa 33; Retinitis Pigmentosa 72; Retinitis Pigmentosa 59; Retinitis Pigmentosa 54; Retinitis Pigmentosa 66; Usher Syndrome Type 1C; Retinitis Pigmentosa Y-Linked; Retinitis Pigmentosa 4; Retinitis Pigmentosa 37; Retinitis Pigmentosa 69; Usher Syndrome Type 1E; Retinitis Pigmentosa 28; Retinitis Pigmentosa 22
Topic Type
group
🧬 Ontology Classifications
DisGeNET Type
group
UMLS Type
Disease or Syndrome
MeSH Class
Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
DO Class
disease of anatomical entity; genetic disease; syndrome
🔗 External References
ICD-10
Disease Ontology
110384; 110376; 110410; 110826;
DisGeNET
C0154860
🔍 Raw view — every non-empty column on this row (26 fields)
name
Hereditary Retinal Dystrophy
alias name
Leber Congenital Amaurosis 4; Retinitis Pigmentosa 50; Retinitis Pigmentosa 77; Leber Congenital Amaurosis 8; Late-Adult Onset Retinitis Pigmentosa; Retinitis Pigmentosa 74; Retinitis Pigmentosa 33; Retinitis Pigmentosa 72; Retinitis Pigmentosa 59; Retinitis Pigmentosa 54; Retinitis Pigmentosa 66; Usher Syndrome Type 1C; Retinitis Pigmentosa Y-Linked; Retinitis Pigmentosa 4; Retinitis Pigmentosa 37; Retinitis Pigmentosa 69; Usher Syndrome Type 1E; Retinitis Pigmentosa 28; Retinitis Pigmentosa 22; Leber Congenital Amaurosis 16; Usher Syndrome Type 1; Retinitis Pigmentosa 19; Retinitis Pigmentos
topic type
group
disgenet disease type
group
umls disease type
Disease or Syndrome
mesh disease class
Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
do disease class
disease of anatomical entity; genetic disease; syndrome
umls disease type id
T047
mesh disease class id
C16; C11
do disease class id
DOID:7; DOID:225; DOID:630
herb disease id
HBDIS003899
disgenet id
C0154860
do id
110384; 110376; 110410; 110826;
icd10 id
H35.5
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How relationships are computed
  • Clinical Trials / Meta-Analyses / References: direct foreign-key link via subject_entity_id (Phase 2d wireup)
  • Formula ↔ Herbs: text bridge via formulas.herbs_in_pinyin matching herbs.pinyin_name
  • Herb ↔ Ingredient: ACTIVE — direct link via herb_ingredients
  • Ingredient ↔ Target: ACTIVE — direct link via ingredient_targets
  • Target ↔ Disease: ACTIVE — direct link via target_health_topics
  • Herb → Target → Disease (full chemical spine): ACTIVE — joins all three link tables