ORPHA:99921

Chronic graft versus host disease

This disease is described under Graft versus host disease

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Chronic graft versus host disease
fr	Maladie chronique du greffon contre l'hôte
de	Graft versus host-Krankheit, chronische
es	Enfermedad crónica de injerto contra hospedador	Enfermedad crónica de injerto versus huésped
it	Malattia cronica del trapianto contro l'ospite
nl	Chronische graft-versus-hostziekte	Chronische GvHD · Chronische GvHZ · Chronische omgekeerde afstotingsziekte · Chronische transplantaat-tegen-gastheerziekte
pt	Doença enxerto versus hospedeiro, crónica
pl	Przewlekła choroba przeszczep przeciwko gospodarzowi
cs	Chronická reakce štěpu proti hostiteli
uk	Хронічна хвороба трансплантат проти хазяїна
zh	慢性移植物抗宿主病
tr	Kronik greft ve konakçı hastalığı

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	T86.0	NTBT	attributed	validated
ICD-11	4B24.1	E	specific	validated
MONDO	0020547	E		validated
UMLS	C0867389	E		validated
GARD	10964	E		validated
MedDRA	10066261	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

ORPHA:39812Graft versus host disease
rare immunological diseases; rare transplant-related disorders

No children.

0 direct

Orphanet records no gene directly on this code.

0 records

No prevalence record in this release.

53 annotations · validated 2024-01-17

HPO	Term (as annotated by Orphanet)	Diagnostic
Very frequent (99-80%)
HP:0007432	Intermittent generalized erythematous papular rash
HP:0001058	Poor wound healing
HP:0001072	Thickened skin
Frequent (79-30%)
HP:0001000	Abnormality of skin pigmentation
HP:0001596	Alopecia
HP:0002110	Bronchiectasis
HP:0002910	Elevated circulating hepatic transaminase concentration
HP:0010783	Erythema
HP:0012537	Food intolerance
HP:0001097	Keratoconjunctivitis sicca
HP:0008404	Nail dystrophy
HP:0001806	Onycholysis
HP:0000613	Photophobia
HP:0000495	Recurrent corneal erosions
HP:0002719	Recurrent infections
HP:0000217	Xerostomia
Occasional (29-5%)
HP:0002027	Abdominal pain
HP:0002031	Abnormal esophagus morphology
HP:0025270	Abnormal esophagus physiology
HP:0000142	Abnormality of the vagina
HP:0006536	Airway obstruction
HP:0002039	Anorexia
HP:0002829	Arthralgia
HP:0001369	Arthritis
HP:0001541	Ascites
HP:0011946	Bronchiolitis obliterans
HP:0100749	Chest pain
HP:0012735	Cough
HP:0002014	Diarrhea
HP:0002015	Dysphagia
HP:0002094	Dyspnea
HP:0012181	Entrapment neuropathy
HP:0002043	Esophageal stricture
HP:0004791	Esophageal ulceration
HP:0100537	Fasciitis
HP:0001371	Flexion contracture
HP:0002020	Gastroesophageal reflux
HP:0000790	Hematuria
HP:0012344	Morphea
HP:0001324	Muscle weakness
HP:0003326	Myalgia
HP:0002018	Nausea
HP:0012531	Pain
HP:0001876	Pancytopenia
HP:0001741	Phimosis
HP:0002202	Pleural effusion
HP:0002107	Pneumothorax
HP:0002113	Pulmonary infiltrates
HP:0200042	Skin ulcer
HP:0200037	Skin vesicle
HP:0100577	Urinary bladder inflammation
HP:0001824	Weight loss
HP:0030828	Wheezing

Annotation source: 12720215[PMID]