about
sea-blue histiocyte syndromeintermittent hydrarthrosismarfanoid–progeroid–lipodystrophy syndromecamptodactyly-arthropathy-coxa vara-pericarditis syndromevasculitis, lymphocytic, nodularretinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndromeconnective tissue disorder due to lysyl hydroxylase-3 deficiencySTAT3-related early-onset multisystem autoimmune diseasehereditary pediatric Behçet-like diseasecalciphylaxis cutishereditary periodic fever syndromemixed autoinflammatory and autoimmune syndromeosteonecrosis of genetic origintype 1 interferonopathyprogeria-associated arthropathycherubismHeredofamilial amyloidosisidiopathic juvenile osteoporosismarfanoidSneddon syndromePAPA syndromeSatoyoshi syndrome
P279
Q18556319-10745368-1101-4483-95AC-C04FF0771DCEQ25345593-5414C5F3-2535-465E-862A-F6988DAEBFCAQ30315066-FDDA9AE0-5D83-4A5C-8EBB-7A40303B7397Q30989065-DC66DA0B-C92C-4637-BB32-564D3BF54C51Q55781600-14F9AC04-5706-4B98-BC8B-A3AE8D58BE05Q55782389-EA8BDD06-0C87-49A7-ACA2-CEBC2F1C18C6Q55783900-D11DC721-3EF0-462E-A4F4-986486B6835FQ55784815-103F6307-8350-48C3-BE94-15E1E54EF233Q55784985-4A322DFB-4844-4288-9284-CCD151273A7EQ55786916-8397B932-9164-4ACC-A2F3-54C06C952FBEQ55787617-0CC39AE7-E0F0-4FC3-94D3-012AE43E48AFQ55787621-F7FA5883-0E7A-4657-812B-2D45B2C26437Q55788020-F64525AD-6399-4BCD-AD76-3A72717570A7Q55788332-9185E4DB-39E4-4472-806B-0DE73F4CF885Q55789415-83173F17-B5FE-4950-9052-529D628C33C7Q568865-EEA5A8E3-692E-4A39-87EF-47B9634F0A50Q5737919-F4780397-DE04-4F88-9DC4-B2EDDB871535Q6318965-6B3F3CB5-CA25-4506-9952-31D065D5E4CDQ6759035-3BBD24BF-94AA-4409-BD5A-FE59ED454D3BQ684840-1DD5DE03-6E20-48AF-A098-86C458097B65Q7118181-4042C29E-3BC6-4F1B-B38C-0142CCFD755CQ7426433-EE4BD8DF-5969-4CF7-A29C-93C6CE4D61C9
P279
description
instance of systemic or rheuma ...... ion of the individual's genome
@en
name
genetic systemic or rheumatologic disease
@en
type
label
genetic systemic or rheumatologic disease
@en
prefLabel
genetic systemic or rheumatologic disease
@en
P1550
P2888
P5270
MONDO:0017133