User:Magnus Manske/Mix'n'match report/405

A report for the Mix'n'match tool. This page will be replaced regularly! Please note:

• If you fix something from this list on Wikidata, please fix it on Mix'n'match as well, if applicable. Otherwise, the error might be re-introduced from there.
• 'External ID' refers to the IDs in the original (external) catalog; the same as the statement value for the associated property.

HPO

Human Phenotype Ontology ID

Unknown external ID

External ID	External label	Item
HP:0000794 HP:0000794		IgA glomerulonephritis (Q1146454)
HP:0001683 HP:0001683		ectopia cordis (Q1356194)
HP:0002083 HP:0002083		migraine without aura (Q3724157)
HP:0003571 HP:0003571		propionic acidemia (Q7250337)
HP:0003978 HP:0003978		radius fracture (Q54911877)
HP:0003987 HP:0003987		ulna fracture (Q47524797)
HP:0004433 HP:0004433		secretory component deficiency (Q55998738)
HP:0004535 HP:0004535		isolated anterior cervical hypertrichosis (Q55782854)
HP:0004809 HP:0004809		neonatal alloimmune thrombocytopenia (Q2622318)
HP:0004864 HP:0004864		sideroblastic anaemia P (Q2610084)
HP:0005191 HP:0005191		Congenital dislocation of the knee (Q16830424)
HP:0005246 HP:0005246		gastric mucosal hypertrophy (Q975705)
HP:0005323 HP:0005323		Friedreich ataxia (Q913856)
HP:0005526 HP:0005526		lymphoid leukemia (Q6708277)
HP:0005527 HP:0005527		congenital high-molecular-weight kininogen deficiency (Q55781893)
HP:0005534 HP:0005534		transient myeloproliferative syndrome (Q32136782)
HP:0005550 HP:0005550		chronic lymphocytic leukemia (Q1088156)
HP:0005679 HP:0005679		Dupuytren's contracture (Q1330254)
HP:0005696 HP:0005696		postaxial polydactyly type A (Q56014345)
HP:0005722 HP:0005722		Hitchhiker's thumb (Q109801820)
HP:0005725 HP:0005725		triphalangeal thumb, Nonopposable (Q55781580)
HP:0005798 HP:0005798		radial Heads, posterior dislocation of (Q55781437)
HP:0005948 HP:0005948		cystic disease of lung (Q55781791)
HP:0006516 HP:0006516		extrinsic allergic alveolitis (Q35890)
HP:0006527 HP:0006527		lymphocytic interstitial pneumonia (Q3907636)
HP:0006688 HP:0006688		paroxysmal tachycardia (Q3980025)
HP:0006702 HP:0006702		idiopathic spontaneous coronary artery dissection (Q55780447)
HP:0006755 HP:0006755		cutaneous leiomyosarcoma (Q18556708)
HP:0006837 HP:0006837		congenital Horner syndrome (Q55950228)
HP:0007406 HP:0007406		hyperpigmentation of eyelid (Q18553782)
HP:0007486 HP:0007486		cavernous hemangioma of face (Q18557005)
HP:0007570 HP:0007570		Hyperkeratosis lenticularis perstans (Q43185102)
HP:0007660 HP:0007660		megalocornea (Q4286595)
HP:0007728 HP:0007728		Microcoria (Q720101)
HP:0007879 HP:0007879		allergic conjunctivitis (Q471521)
HP:0007947 HP:0007947		autosomal recessive pericentral pigmentary retinopathy (Q27677820)
HP:0008051 HP:0008051		abnormality of retinal pigmentation (Q29643939)
HP:0008459 HP:0008459		cervical vertebrae, agenesis of (Q55781739)
HP:0008469 HP:0008469		cervical vertebral dysplasia (Q55780412)
HP:0008480 HP:0008480		spondylosis (Q1097028)
HP:0008653 HP:0008653		crescentic glomerulonephritis (Q18554448)
HP:0008682 HP:0008682		acute kidney tubular necrosis (Q2425407)
HP:0008711 HP:0008711		prostatic hypertrophy (Q506659)
HP:0008718 HP:0008718		renal dysplasia, unilateral (Q55788766)
HP:0008940 HP:0008940		persistent generalized lymphadenopathy (Q7170411)
HP:0009037 HP:0009037		spinal muscular atrophy, segmental (Q55781491)
HP:000962 HP:000962		hyperkeratosis (Q1640998)
HP:0009812 HP:0009812		abrachia (Q2565692)
HP:0009818 HP:0009818		amelia of lower limb (Q55787050)
HP:0009900 HP:0009900		unilateral hearing loss (Q3813334)
HP:0009920 HP:0009920		nevus of Ota (Q2053690)
HP:0009938 HP:0009938		sunken cheeks (Q29642730)
HP:0010313 HP:0010313		juvenile macromastia (Q3144218)
HP:0010448 HP:0010448		colonic atresia (Q55782541)
HP:0010474 HP:0010474		bladder calculus (Q3825881)
HP:0010498 HP:0010498		Patella bipartita (Q2056680)
HP:0010518 HP:0010518		thyroglossal cyst (Q502785)
HP:0010525 HP:0010525		finger agnosia (Q1114480)
HP:0010527 HP:0010527		astereognosia (Q739221)
HP:0010528 HP:0010528		prosopagnosia (Q244438)
HP:0010533 HP:0010533		Spasmus nutans (Q9340085)
HP:0010542 HP:0010542		vestibular nystagmus (Q18554676)
HP:0010605 HP:0010605		meibomian cyst (Q769595)
HP:0010606 HP:0010606		hordeolum (Q202173)
HP:0010736 HP:0010736		Monostotic fibrous dysplasia (Q6901991)
HP:0010865 HP:0010865		oppositional defiant disorder (Q1328833)
HP:0010896 HP:0010896		sarcosinemia (Q7423635)
HP:0010906 HP:0010906		histidinemia (Q725845)
HP:0010910 HP:0010910		Hypervalinemia (Q5958808)
HP:0010941 HP:0010941		nasal bones, absence of (Q55781269)
HP:0010943 HP:0010943		echogenic bowel (Q55190262)
HP:0010945 HP:0010945		Pyelectasis (Q7262961)
HP:0010958 HP:0010958		bilateral renal aplasia (Q44743904)
HP:0010959 HP:0010959		congenital cystic adenomatoid malformation (Q246040)
HP:0010960 HP:0010960		pulmonary sequestration (Q688890)
HP:0010992 HP:0010992		stress incontinence (Q3797702)
HP:0011067 HP:0011067		hyperdontia (Q542946)
HP:0011088 HP:0011088		Dens invaginatus (Q3847228)
HP:0011110 HP:0011110		tonsillitis (Q186470)
HP:0011142 HP:0011142		early-onset nuclear cataract (Q56014424)
HP:0011286 HP:0011286		Hirschsprung's disease (Q1343645)
HP:0011331 HP:0011331		Parry–Romberg syndrome (Q250365)
HP:0011333 HP:0011333		Asymmetric crying facies (Q4812072)
HP:0011369 HP:0011369		Mongolian spot (Q1072716)
HP:0011418 HP:0011418		Vasa praevia (Q1899576)
HP:0011419 HP:0011419		placental abruption (Q388113)
HP:0011444 HP:0011444		decerebration (Q1207349)
HP:0011533 HP:0011533		snowflake vitreoretinal degeneration (Q55345684)
HP:0011540 HP:0011540		levo-transposition of the great arteries (Q1784755)
HP:0011566 HP:0011566		cor triatriatum dexter (Q55789362)
HP:0011567 HP:0011567		Sinus venosus atrial septal defect (Q7525206)
HP:0011570 HP:0011570		congenital mitral stenosis (Q55789331)
HP:0011604 HP:0011604		Aortopulmonary window (Q616089)
HP:0011627 HP:0011627		aorto-ventricular tunnel (Q55787720)
HP:0011665 HP:0011665		takotsubo cardiomyopathy (Q595907)
HP:0011700 HP:0011700		ectopic atrial tachycardia (Q54946755)
HP:0011701 HP:0011701		multifocal atrial tachycardia (Q1165996)
HP:0011709 HP:0011709		heart conduction disease (Q1361515)
HP:0011716 HP:0011716		junctional ectopic tachycardia (Q3513620)
HP:0011724 HP:0011724		arrhythmogenic right ventricular dysplasia 1 (Q2852241)
HP:0011726 HP:0011726		persistent fetal circulation syndrome (Q7170410)
HP:0011763 HP:0011763		pituitary carcinoma (Q18556544)
HP:0011771 HP:0011771		autoimmune hypoparathyroidism (Q55787815)
HP:0011779 HP:0011779		anaplastic thyroid carcinoma (Q19000862)
HP:0011782 HP:0011782		thyroid crisis (Q4458080)
HP:0011798 HP:0011798		renal oncocytoma (Q3882418)
HP:0011841 HP:0011841		ventricular flutter (Q460864)
HP:0011846 HP:0011846		osteoblastoma (Q1807280)
HP:0011851 HP:0011851		hemopericardium (Q3144949)
HP:0011854 HP:0011854		hemoperitoneum (Q1510899)
HP:0011856 HP:0011856		pica (Q1134891)
HP:0011857 HP:0011857		plasmacytoma (Q2090167)
HP:0011868 HP:0011868		sciatica (Q565276)
HP:0011874 HP:0011874		heparin-induced thrombocytopenia (Q1598365)
HP:0011886 HP:0011886		hyphema (Q1298559)
HP:0011887 HP:0011887		intraventricular hemorrhage (Q6058597)
HP:0011891 HP:0011891		postpartum hemorrhage (Q2916482)
HP:0011919 HP:0011919		pleural empyema (Q200781)
HP:0011920 HP:0011920		hydrothorax (Q1505538)
HP:0011946 HP:0011946		bronchiolitis obliterans (Q614750)
HP:0012005 HP:0012005		déjà vu (Q158103)
HP:0012022 HP:0012022		patent ductus venosus (Q55783186)
HP:0012063 HP:0012063		Aneurysmal bone cyst (Q4761773)
HP:0012076 HP:0012076		borderline personality disorder (Q208166)
HP:0012077 HP:0012077		histrionic personality disorder (Q845787)
HP:0012085 HP:0012085		pyuria (Q778731)
HP:0012089 HP:0012089		arteritis (Q1751810)
HP:0012121 HP:0012121		panuveitis (Q18554228)
HP:0012124 HP:0012124		intermediate uveitis (Q8511208)
HP:0012154 HP:0012154		anhedonia (Q545365)
HP:0012159 HP:0012159		internal carotid artery dissection (Q54928207)
HP:0012170 HP:0012170		nail biting (Q1367423)
HP:0012193 HP:0012193		anaplastic large-cell lymphoma (Q486090)
HP:0012196 HP:0012196		cheyne-stokes respiration (Q1071481)
HP:0012199 HP:0012199		cluster headache (Q166907)
HP:0012281 HP:0012281		chylous ascites (Q15727012)
HP:0012290 HP:0012290		mouth cancer (Q1143025)
HP:0012317 HP:0012317		arthritis, Sacroiliac (Q55780347)
HP:0012318 HP:0012318		occipital neuralgia (Q3347239)
HP:0012328 HP:0012328		cementoma (Q4503868)
HP:0012329 HP:0012329		tufted angioma (Q2849604)
HP:0012333 HP:0012333		abnormal sudomotor regulation (Q56565058)
HP:0012370 HP:0012370		visible zygomatic arches (Q43166127)
HP:0012390 HP:0012390		anal fissure (Q484797)
HP:0012395 HP:0012395		seasonal allergic rhinitis (Q3740609)
HP:0012396 HP:0012396		biliary dyskinesia (Q2028354)
HP:0012399 HP:0012399		pressure ulcer (Q308978)
HP:0012410 HP:0012410		pure red-cell aplasia (Q751631)
HP:0012413 HP:0012413		congenital syphilis (Q5160454)
HP:0012416 HP:0012416		hypercapnia (Q615759)
HP:0012417 HP:0012417		hypocapnia (Q1328215)
HP:0012424 HP:0012424		chorioretinitis (Q1402851)
HP:0012441 HP:0012441		Sphincter of Oddi dysfunction (Q4162400)
HP:0012446 HP:0012446		cerebral folate receptor alpha deficiency (Q18553424)
HP:0012452 HP:0012452		restless legs syndrome (Q916280)
HP:0012459 HP:0012459		primary headache disorder (Q54927701)
HP:0012461 HP:0012461		bacteriuria (Q632522)
HP:0012462 HP:0012462		geniospasm (Q3816650)
HP:0012481 HP:0012481		central nervous system venous angioma (Q54974116)
HP:0012486 HP:0012486		myelitis (Q551085)
HP:0012498 HP:0012498		nuchal cord (Q1961969)
HP:0012533 HP:0012533		hyperalgesia (Q1633866)
HP:0012579 HP:0012579		lipoid nephrosis (Q1323002)
HP:0012582 HP:0012582		renal dysplasia, bilateral (Q55788767)
HP:0012618 HP:0012618		Urachal cyst (Q7899540)
HP:0012636 HP:0012636		retinal vein occlusion (Q18554884)
HP:0012652 HP:0012652		exercise-induced bronchoconstriction (Q5420019)
HP:0012653 HP:0012653		status asthmaticus (Q826759)
HP:0012705 HP:0012705		Abnormal metabolic brain imaging by MRS (Q29643776)
HP:0012706 HP:0012706		Elevated brain choline level by MRS (Q29643793)
HP:0012708 HP:0012708		Reduced brain N-acetyl aspartate level by MRS (Q56565032)
HP:0012710 HP:0012710		ingrown nail (Q1060425)
HP:0012723 HP:0012723		sinoatrial block (Q1426241)
HP:0012784 HP:0012784		perinephritis (Q4344969)
HP:0012803 HP:0012803		anisometropia (Q247978)
HP:0012824 HP:0012824		severity (Q96278582)
HP:0012825 HP:0012825		mild (Q96278776)
HP:0012826 HP:0012826		moderate (Q96280403)
HP:0012828 HP:0012828		severe (Q96280471)
HP:0012859 HP:0012859		esophageal leukoplakia (Q18558047)
HP:0012876 HP:0012876		premature ejaculation (Q319312)
HP:0025004 HP:0025004		hallux rigidus (Q1425208)
HP:0025019 HP:0025019		arterial rupture (Q110930434)
HP:0025044 HP:0025044		lung abscess (Q1877550)
HP:0025059 HP:0025059		splenic abscess (Q18555108)
HP:0025105 HP:0025105		Nevus oligemicus (Q16896971)
HP:0025107 HP:0025107		cutis marmorata telangiectatica congenita (Q1997180)
HP:0025127 HP:0025127		actinic keratosis (Q422225)
HP:0025143 HP:0025143		chills (Q2260058)
HP:0025171 HP:0025171		rosette-forming glioneuronal tumor (Q104640155)
HP:0025197 HP:0025197		Infantile digital fibromatosis (Q16917828)
HP:0025314 HP:0025314		Choroidal nevus (Q112811902)
HP:0025420 HP:0025420		diffuse alveolar hemorrhage (Q55788710)
HP:0025455 HP:0025455		Decreased CSF 5-hydroxyindolacetic acid (Q30150977)
HP:0025457 HP:0025457		Decreased CSF total protein (Q30151275)
HP:0025458 HP:0025458		Decreased CSF albumin (Q30150991)
HP:0025460 HP:0025460		High myoinositol in brain by MRS (Q30151297)
HP:0025471 HP:0025471		congenital panfollicular nevus (Q55785409)
HP:0025488 HP:0025488		detrusor sphincter dyssynergia (Q13629899)
HP:0025569 HP:0025569		polypoidal choroidal vasculopathy (Q113586103)
HP:0025599 HP:0025599		over elevation in adduction (Q1677078)
HP:0025613 HP:0025613		affective seizure (Q12761940)
HP:0025643 HP:0025643		Tarlov cyst (Q1648960)
HP:0030001 HP:0030001		lagophthalmos (Q620918)
HP:0030003 HP:0030003		paralytic lagophthalmos (Q18554408)
HP:0030004 HP:0030004		cicatricial lagophthalmos (Q18554421)
HP:0030009 HP:0030009		cervical incompetence (Q2563414)
HP:0030017 HP:0030017		vaginismus (Q1128431)
HP:0030028 HP:0030028		nasal bones, absence of (Q55781269)
HP:0030064 HP:0030064		central neurocytoma (Q5062123)
HP:0030068 HP:0030068		esthesioneuroblastoma (Q256806)
HP:0030072 HP:0030072		paranasal sinus neoplasm (Q18554532)
HP:0030075 HP:0030075		intraductal carcinoma (Q337585)
HP:0030076 HP:0030076		breast carcinoma in situ (Q18558015)
HP:0030077 HP:0030077		bronchial neoplasm (Q18556111)
HP:0030149 HP:0030149		cardiogenic shock (Q2477062)
HP:0030158 HP:0030158		cervix erosion (Q720523)
HP:0030159 HP:0030159		cervical polyp (Q5065349)
HP:0030207 HP:0030207		Flail chest (Q1061988)
HP:0030219 HP:0030219		semantic dementia (Q18587)
HP:0030222 HP:0030222		visual agnosia (Q18742)
HP:0030248 HP:0030248		mesenteric ischemia (Q221463)
HP:0030357 HP:0030357		lung small cell carcinoma (Q19000544)
HP:0030393 HP:0030393		endolymphatic sac tumor (Q5376356)
HP:0030403 HP:0030403		platelet aggregation, spontaneous (Q55781376)
HP:0030407 HP:0030407		Pineocytoma (Q17106360)
HP:0030411 HP:0030411		jejunal adenocarcinoma (Q18553569)
HP:0030416 HP:0030416		vulvar cancer (Q1908194)
HP:0030418 HP:0030418		vulvar melanoma (Q18554991)
HP:0030419 HP:0030419		Bartholin's gland carcinoma (Q18556143)
HP:0030426 HP:0030426		ossifying fibroma (Q7107615)
HP:0030429 HP:0030429		nasopharyngeal angiofibroma (Q546357)
HP:0030430 HP:0030430		neuroma (Q1981345)
HP:0030432 HP:0030432		chondroblastoma (Q1076053)
HP:0030433 HP:0030433		osteoid osteoma (Q1473802)
HP:0030439 HP:0030439		anal canal adenocarcinoma (Q18556025)
HP:0030447 HP:0030447		Merkel cell carcinoma (Q1711744)
HP:0030451 HP:0030451		mesenteric cyst (Q6821207)
HP:0030642 HP:0030642		fundus albipunctatus (Q16570127)
HP:0030673 HP:0030673		Wagner's disease (Q2470609)
HP:0030706 HP:0030706		ranula (Q1756640)
HP:0030711 HP:0030711		hydrocolpos (Q5954725)
HP:0030712 HP:0030712		gynatresia (Q1486140)
HP:0030713 HP:0030713		Vein of Galen aneurysmal malformations (Q11766796)
HP:0030764 HP:0030764		ochronosis (Q1507609)
HP:0030765 HP:0030765		night horror (Q849736)
HP:0030766 HP:0030766		otalgia (Q1596398)
HP:0030767 HP:0030767		Epignathus (Q55785438)
HP:0030770 HP:0030770		craniorachischisis (Q55788430)
HP:0030784 HP:0030784		anomic aphasia (Q567576)
HP:0030792 HP:0030792		jaw cancer (Q18554922)
HP:0030803 HP:0030803		Platonychia (Q7202439)
HP:0030811 HP:0030811		glossalgia (Q1532173)
HP:0030816 HP:0030816		gingival recession (Q964920)
HP:0030833 HP:0030833		neck pain (Q3567802)
HP:0030834 HP:0030834		shoulder pain (Q55105885)
HP:0030854 HP:0030854		scleral staphyloma (Q18554116)
HP:0030858 HP:0030858		addictive behavior (Q4681134)
HP:0030883 HP:0030883		femoral acetabular impingement (Q1910771)
HP:0030906 HP:0030906		sucking reflex (Q2227392)
HP:0030978 HP:0030978		Decreased CSF/serum albumin ratio (Q30150985)
HP:0030980 HP:0030980		Reduced brain glutamine level by MRS (Q56565037)
HP:0031009 HP:0031009		ainhum (Q2161046)
HP:0031013 HP:0031013		ankylosis (Q418418)
HP:0031018 HP:0031018		Syringofibroadenoma (Q7663357)
HP:0031025 HP:0031025		gastric leiomyosarcoma (Q18556713)
HP:0031051 HP:0031051		Tarsal sclerosis (Q30150584)
HP:0031058 HP:0031058		impaired daily living skills (Q56565019)
HP:0031107 HP:0031107		Decreased fibular diameter (Q30150526)
HP:0031146 HP:0031146		Impaired oral bolus formation (Q56565094)
HP:0031161 HP:0031161		Reduced brain glutamate level by MRS (Q56565041)
HP:0031162 HP:0031162		Impaired oropharyngeal swallow response (Q56565097)
HP:0031369 HP:0031369		colon perforation (Q110930564)
HP:0031493 HP:0031493		glandular cell epithelial neoplasm (Q18968206)
HP:0032505 HP:0032505		hydrophobia (sign) (Q56635009)
HP:0032508 HP:0032508		Polyembolokoilamania (Q106678847)
HP:0033845 HP:0033845		sense of impending doom (Q110222715)
HP:0040113 HP:0040113		presbycusis (Q1756133)
HP:0040141 HP:0040141		tardive dyskinesia (Q1546328)
HP:0040150 HP:0040150		epiblepharon (Q3726816)
HP:0040184 HP:0040184		oral hemorrhage (Q54946292)
HP:0040192 HP:0040192		Apudoma (Q3621073)
HP:0040197 HP:0040197		encephalomalacia (Q947813)
HP:0040209 HP:0040209		Decreased CSF biopterin level (Q29643842)
HP:0040233 HP:0040233		factor Xiii, a subunit, deficiency of (Q56002513)
HP:0040234 HP:0040234		factor Xiii, b subunit, deficiency of (Q56002515)
HP:0040262 HP:0040262		serous glue ear (Q2058432)
HP:0045029 HP:0045029		Eosinophilic fasciitis (Q2325206)
HP:0045041 HP:0045041		glycogen storage disease due to lactate dehydrogenase H-subunit deficiency (Q55784190)
HP:0100002 HP:0100002		benign pleural mesothelioma (Q18556653)
HP:0100003 HP:0100003		peritoneal mesothelioma (Q7168876)
HP:0100004 HP:0100004		pericardial mesothelioma (Q18557171)
HP:0100029 HP:0100029		Lingual Thyroid (Q54935336)
HP:0100310 HP:0100310		epidural cranial hematoma (Q2716919)
HP:0100497 HP:0100497		pellagra (Q221441)
HP:0100507 HP:0100507		folate deficiency (Q2915477)
HP:0100510 HP:0100510		ascorbic acid deficiency (Q18967616)
HP:0100551 HP:0100551		tracheal neoplasm (Q7831293)
HP:0100575 HP:0100575		gallbladder cancer (Q977787)
HP:0100577 HP:0100577		cystitis (Q246084)
HP:0100588 HP:0100588		paraphimosis (Q1414480)
HP:0100595 HP:0100595		idiopathic camptocormia (Q55785363)
HP:0100600 HP:0100600		penoscrotal transposition (Q55786963)
HP:0100604 HP:0100604		lip cancer (Q4389274)
HP:0100616 HP:0100616		testicular teratoma (Q53910645)
HP:0100628 HP:0100628		Zenker's diverticulum (Q189638)
HP:0100661 HP:0100661		trigeminal neuralgia (Q1132120)
HP:0100677 HP:0100677		vulval varices (Q55789762)
HP:0100695 HP:0100695		lipedema (Q1827605)
HP:0100739 HP:0100739		bulimia nervosa (Q180913)
HP:0100746 HP:0100746		macrodactylia of fingers (Q18966921)
HP:0100747 HP:0100747		macrodactylia of toes (Q18966807)
HP:0100757 HP:0100757		pancreatoblastoma (Q7130423)
HP:0100762 HP:0100762		Haemobilia (Q1642116)
HP:0100768 HP:0100768		choriocarcinoma (Q1076481)
HP:0100808 HP:0100808		gastric diverticulum (Q40943828)
HP:0100812 HP:0100812		halitosis (Q16408)
HP:0100822 HP:0100822		rectocele (Q964891)
HP:0100844 HP:0100844		pancreatic fistula (Q7130409)
HP:0100845 HP:0100845		anaphylaxis (Q168800)
HP:0100890 HP:0100890		choledochal cyst (Q2027937)
HP:0100924 HP:0100924		Sclerosis of toe phalanx (Q30151307)
HP:0400007 HP:0400007		polymenorrhea (Q3395659)
HP:0410030 HP:0410030		cleft lip (Q12050056)
HP:0410170 HP:0410170		hippocampal atrophy (Q110929303)
HP:0410279 HP:0410279		pituitary atrophy (Q12762697)
HP:0500006 HP:0500006		urethritis (Q1122485)
HP:0500021 HP:0500021		Reduced brain gamma-aminobutyric acid level by MRS (Q56565048)
HP:0500021 HP:0500021		Reduced brain gamma-aminobutyric acid level by MRS (Q30151286)
class of which this subject is a particular example and member that class of which this subject is a particular example and member		Deepak Pun Magar (Q106916265)

Different items for the same external ID

External ID	External label	Item in Wikidata	Item in Mix'n'Match	Mix'n'match entry
HP:0001263 HP:0001263	Global developmental delay	global developmental delay (Q25312637)	developmental disability (Q1142806)	19252470
HP:0001369 HP:0001369	Arthritis	joint inflammation (Q102186573)	arthritis (Q170990)	19250589
HP:0001388 HP:0001388	Joint laxity	ligamentous laxity (Q6545848)	hypermobility syndrome (Q1641042)	19253320
HP:0001395 HP:0001395	Hepatic fibrosis	liver fibrosis (Q3071321)	liver cirrhosis (Q147778)	19252594
HP:0004305 HP:0004305	Involuntary movements	involuntary movement (Q11361883)	movement disorders (Q2608695)	19253265
HP:0006495 HP:0006495	Aplasia/Hypoplasia of the ulna	ulnar dysplasia (Q112160984)	Aplasia/Hypoplasia of the ulna (Q110931183)	19250535
HP:0009725 HP:0009725	Bladder neoplasm	bladder neoplasm (Q55949884)	bladder cancer (Q504775)	19250780

Same item for multiple external IDs in Mix'n'match

Item in Mix'n'Match	Mix'n'match entry	External ID	External label
liver cirrhosis (Q147778)	19251163	HP:0001394 HP:0001394	Cirrhosis
	19252594	HP:0001395 HP:0001395	Hepatic fibrosis
baldness (Q181391)	19252330	HP:0002292 HP:0002292	Frontal balding
	19250232	HP:0002293 HP:0002293	Alopecia of scalp
stomach cancer (Q189588)	19254072	HP:0006753 HP:0006753	Neoplasm of the stomach
	19255680	HP:0012126 HP:0012126	Stomach cancer
hypoglycemia (Q202758)	19252818	HP:0001943 HP:0001943	Hypoglycemia
	19252190	HP:0003162 HP:0003162	Fasting hypoglycemia
acute myeloid leukemia (Q264118)	19250153	HP:0004808 HP:0004808	Acute myeloid leukemia
	19250151	HP:0006733 HP:0006733	Acute megakaryocytic leukemia
abducens nerve palsy (Q317977)	19251382	HP:0006897 HP:0006897	Cranial nerve VI palsy
	19248846	HP:0011349 HP:0011349	Abducens palsy
craniosynostosis (Q378183)	19256009	HP:0000243 HP:0000243	Trigonocephaly
	19256025	HP:0000262 HP:0000262	Turricephaly
	19254296	HP:0000263 HP:0000263	Oxycephaly
	19251393	HP:0001363 HP:0001363	Craniosynostosis
retinal disease (Q550455)	19249863	HP:0000479 HP:0000479	Abnormality of the retina
	19255210	HP:0000488 HP:0000488	Retinopathy
hip dysplasia (Q625935)	19251272	HP:0001374 HP:0001374	Congenital hip dislocation
	19252636	HP:0001385 HP:0001385	Hip dysplasia
biliary atresia (Q659033)	19252143	HP:0005242 HP:0005242	Extrahepatic biliary duct atresia
	19250761	HP:0005912 HP:0005912	Biliary atresia
arthropathy (Q708176)	19248989	HP:0001367 HP:0001367	Abnormal joint morphology
	19250591	HP:0003040 HP:0003040	Arthropathy
respiratory failure (Q767485)	19255156	HP:0002093 HP:0002093	Respiratory insufficiency
	19255154	HP:0002878 HP:0002878	Respiratory failure
gait abnormality (Q827017)	19252369	HP:0001288 HP:0001288	Gait disturbance
	19255588	HP:0002064 HP:0002064	Spastic gait
aplastic anemia (Q846316)	19252910	HP:0001908 HP:0001908	Hypoplastic anemia
	19250553	HP:0001915 HP:0001915	Aplastic anemia
hypogonadism (Q938107)	19252826	HP:0000044 HP:0000044	Hypogonadotrophic hypogonadism
	19252825	HP:0000135 HP:0000135	Hypogonadism
	19252706	HP:0000815 HP:0000815	Hypergonadotropic hypogonadism
optic neuritis (Q972514)	19254221	HP:0100653 HP:0100653	Optic neuritis
	19255212	HP:0100654 HP:0100654	Retrobulbar optic neuritis
agammaglobulinemia (Q1047559)	19251472	HP:0004313 HP:0004313	Decreased antibody level in blood
	19250194	HP:0004432 HP:0004432	Agammaglobulinemia
kidney disease (Q1054718)	19249704	HP:0000077 HP:0000077	Abnormality of the kidney
	19254086	HP:0000112 HP:0000112	Nephropathy
hemolytic anemia (Q1145668)	19252579	HP:0001878 HP:0001878	Hemolytic anemia
	19253776	HP:0001937 HP:0001937	Microangiopathic hemolytic anemia
interstitial lung disease (Q1153419)	19253229	HP:0006515 HP:0006515	Interstitial pneumonitis
	19253230	HP:0006530 HP:0006530	Interstitial pulmonary abnormality
acute liver failure (Q1192530)	19252348	HP:0004448 HP:0004448	Fulminant hepatic failure
	19250144	HP:0006554 HP:0006554	Acute hepatic failure
encephalocele (Q1346023)	19251985	HP:0002084 HP:0002084	Encephalocele
	19254171	HP:0002085 HP:0002085	Occipital encephalocele
fasciculation (Q1397878)	19255938	HP:0001308 HP:0001308	Tongue fasciculations
	19252187	HP:0002380 HP:0002380	Fasciculations
interstitial nephritis (Q1424106)	19256022	HP:0001969 HP:0001969	Tubulointerstitial abnormality
	19256024	HP:0001970 HP:0001970	Tubulointerstitial nephritis
piebaldism (Q1516083)	19254391	HP:0007443 HP:0007443	Partial albinism
	19254539	HP:0007544 HP:0007544	Piebaldism
renal tubular acidosis (Q1516211)	19255144	HP:0001947 HP:0001947	Renal tubular acidosis
	19254872	HP:0002049 HP:0002049	Proximal renal tubular acidosis
Glanzmann's thrombasthenia (Q1529258)	19249969	HP:0001872 HP:0001872	Abnormality of thrombocytes
	19251533	HP:0001975 HP:0001975	Decreased platelet glycoprotein IIb-IIIa
hydrophthalmos (Q1640324)	19250912	HP:0000557 HP:0000557	Buphthalmos
	19251269	HP:0001087 HP:0001087	Congenital glaucoma
ophthalmoplegia (Q1723331)	19254205	HP:0000597 HP:0000597	Ophthalmoparesis
	19254206	HP:0000602 HP:0000602	Ophthalmoplegia
spinal cord disease (Q2303951)	19249893	HP:0002143 HP:0002143	Abnormality of the spinal cord
	19253951	HP:0002196 HP:0002196	Myelopathy
scimitar syndrome (Q2557206)	19255949	HP:0005160 HP:0005160	Total anomalous pulmonary venous return
	19250299	HP:0010772 HP:0010772	Anomalous pulmonary venous return
movement disorders (Q2608695)	19253265	HP:0004305 HP:0004305	Involuntary movements
	19249380	HP:0100022 HP:0100022	Abnormality of movement
retinal degeneration (Q3043268)	19255186	HP:0000546 HP:0000546	Retinal degeneration
	19255181	HP:0001105 HP:0001105	Retinal atrophy
3-methylglutaconic aciduria (Q3598794)	19248830	HP:0003344 HP:0003344	3-Methylglutaric aciduria
	19248829	HP:0003535 HP:0003535	3-Methylglutaconic aciduria
basal ganglia disease (Q4866181)	19249280	HP:0002071 HP:0002071	Abnormality of extrapyramidal motor function
	19249523	HP:0002134 HP:0002134	Abnormality of the basal ganglia
palmoplantar keratosis (Q7128426)	19254314	HP:0000972 HP:0000972	Palmoplantar hyperkeratosis
	19254315	HP:0000982 HP:0000982	Palmoplantar keratoderma
pituitary gland disease (Q7199538)	19249507	HP:0011747 HP:0011747	Abnormality of the anterior pituitary
	19249824	HP:0012503 HP:0012503	Abnormality of the pituitary gland
thyroid dysgenesis (Q7799746)	19255913	HP:0005990 HP:0005990	Thyroid hypoplasia
	19255909	HP:0008188 HP:0008188	Thyroid dysgenesis
ovotesticular disorder of sex development (Q54944059)	19256015	HP:0010459 HP:0010459	True hermaphroditism
	19254295	HP:0012861 HP:0012861	Ovotestis
Craniosynostosis, Philadelphia type: a new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toes (Q56384030)	19248821	HP:0004691 HP:0004691	2-3 toe syndactyly
	19248824	HP:0010714 HP:0010714	2-4 toe syndactyly
1-5 finger complete cutaneous syndactyly (Q106439943)	19248815	HP:0006088 HP:0006088	1-5 finger complete cutaneous syndactyly
	19248816	HP:0010708 HP:0010708	1-5 finger syndactyly

Multiple items for the same external ID in Wikidata

External ID	Items in Mix'n'Match
HP:0001263 HP:0001263	developmental disability (Q1142806) global developmental delay (Q25312637)
HP:0001369 HP:0001369	arthritis (Q170990) joint inflammation (Q102186573)
HP:0001388 HP:0001388	hypermobility syndrome (Q1641042) ligamentous laxity (Q6545848)
HP:0001395 HP:0001395	liver cirrhosis (Q147778) liver fibrosis (Q3071321)
HP:0006495 HP:0006495	Aplasia/Hypoplasia of the ulna (Q110931183) ulnar dysplasia (Q112160984)
HP:0009725 HP:0009725	bladder cancer (Q504775) bladder neoplasm (Q55949884)
HP:0500021 HP:0500021	Reduced brain gamma-aminobutyric acid level by MRS (Q30151286) Reduced brain gamma-aminobutyric acid level by MRS (Q56565048)