2018-02-19 release (multiple new rare diseases)

This release incorporates many more rare diseases from the globalgenes rare list. Not all of these newly added terms are yet fully curated

New Terms

• MONDO:0021722 ! vulvodynia
• MONDO:0021723 ! vaginismus
• MONDO:0021725 ! Abderhalden-Kaufmann-Lignac syndrome
• MONDO:0021726 ! abdominal cystic lymphangioma
• MONDO:0021727 ! aberrant subclavian artery
• MONDO:0021745 ! psychosocial short stature
• MONDO:0021747 ! acanthamoeba infectious disease
• MONDO:0021752 ! Achard-Thiers syndrome
• MONDO:0021758 ! acquired agranulocytosis
• MONDO:0021759 ! acquired fructose intolerance
• MONDO:0021761 ! acral dysostosis dyserythropoiesis syndrome
• MONDO:0021762 ! acro coxo mesomelic dysplasia
• MONDO:0021764 ! acrofacial dysostosis preis type
• MONDO:0021805 ! acromesomelic dysplasia, Campailla Martinelli type
• MONDO:0021808 ! acute cholinergic dysautonomia
• MONDO:0021809 ! primary dysautonomia
• MONDO:0021811 ! acute mountain sickness
• MONDO:0021812 ! adnexal spiradenoma/cylindroma of a sweat gland
• MONDO:0021824 ! adult progressive spinal muscular atrophy, Aran Duchenne type
• MONDO:0021826 ! aerobic actinomyces infection
• MONDO:0021829 ! agnathia-microstomia-synotia
• MONDO:0021834 ! akaba hayasaka syndrome
• MONDO:0021836 ! aksu von stockhausen syndrome
• MONDO:0021838 ! Al Gazali Khidr Prem Chandran syndrome
• MONDO:0021845 ! Aloi Tomasini Isaia syndrome
• MONDO:0021849 ! alopecia macular degeneration growth retardation syndome
• MONDO:0021851 ! alopecia universalis onychodystrophy vitiligo
• MONDO:0021856 ! Alsing syndrome
• MONDO:0021879 ! anaplastic small cell lymphoma
• MONDO:0021896 ! anterior spinal artery stroke
• MONDO:0021902 ! aortopulmonary window
• MONDO:0021905 ! Apert-like polydactyly syndrome
• MONDO:0021907 ! aplasia cutis autosomal recessive
• MONDO:0021908 ! aplasia cutis congenita dominant
• MONDO:0021909 ! aplasia cutis congenita recessive
• MONDO:0021910 ! aplasia cutis myopia
• MONDO:0021913 ! aquagenic pruritus
• MONDO:0021915 ! arakawa syndrome 2
• MONDO:0021918 ! arena syndrome
• MONDO:0021921 ! arnold stickler bourne syndrome
• MONDO:0021923 ! Arroyo Garcia Cimadevilla syndrome
• MONDO:0021927 ! arthrogryposis epileptic seizures migrational brain disorder
• MONDO:0021935 ! aspergillus niger infection
• MONDO:0021937 ! Asrar Facharzt Haque syndrome
• MONDO:0021944 ! auditory neuropathy
• MONDO:0021945 ! hearing disorder
• MONDO:0021950 ! autoimmune oophoritis
• MONDO:0021952 ! autoimmune progesterone dermatitis
• MONDO:0021957 ! autosomal recessive nonsyndromic congenital nuclear cataract
• MONDO:0021962 ! baetz-greenwalt syndrome
• MONDO:0021964 ! bagatelle cassidy syndrome
• MONDO:0021966 ! Baker Vinters syndrome
• MONDO:0021969 ! Banti syndrome
• MONDO:0021971 ! Baraitser Rodeck Garner syndrome
• MONDO:0021977 ! basaloid follicular hamartoma
• MONDO:0021979 ! Basaran Yilmaz syndrome
• MONDO:0021994 ! Berk-Tabatznik syndrome
• MONDO:0022011 ! bobble-head doll syndrome
• MONDO:0022013 ! Boerhaave syndrome
• MONDO:0022018 ! Borrone di Rocco Crovato syndrome
• MONDO:0022020 ! boudhina yedes khiari syndrome
• MONDO:0022022 ! bowenoid papulosis
• MONDO:0022025 ! boylan dew greco syndrome
• MONDO:0022055 ! Calabro syndrome
• MONDO:0022057 ! calcifying epithelial odontogenic tumor
• MONDO:0022060 ! calloso-genital dysplasia
• MONDO:0022067 ! cantu sanchez-corona fragoso syndrome
• MONDO:0022070 ! cantu sanchez-corona hernandez syndrome
• MONDO:0022071 ! carbon baby syndrome
• MONDO:0022089 ! carnevale hernandez castillo syndrome
• MONDO:0022094 ! Cartwright Nelson Fryns syndrome
• MONDO:0022098 ! catamenial pneumothorax
• MONDO:0022109 ! catatrichy
• MONDO:0022113 ! central centrifugal cicatricial alopecia
• MONDO:0022140 ! Charles Bonnet syndrome
• MONDO:0022151 ! Chitty Hall Webb syndrome
• MONDO:0022171 ! chromhidrosis
• MONDO:0022173 ! chromosome 11q trisomy
• MONDO:0022174 ! chromosome 12p deletion
• MONDO:0022177 ! chromosome 13q trisomy
• MONDO:0022178 ! chromosome 13q-mosaicism
• MONDO:0022180 ! chromosome 16 trisomy
• MONDO:0022196 ! chronic erosive gastritis
• MONDO:0022200 ! treatment for disease
• MONDO:0022201 ! has treatment by surgery
• MONDO:0022236 ! colpocephaly
• MONDO:0022263 ! congenital hepatic fibrosis
• MONDO:0022266 ! congenital hepatic fibrosis
• MONDO:0022267 ! congenital herpes simplex
• MONDO:0022308 ! corticobasal degeneration disorder
• MONDO:0022311 ! cote katsantoni syndrome
• MONDO:0022314 ! Hernandez Aguirre-Negrete syndrome
• MONDO:0022316 ! hair defect with photosensitivity and intellectual disability syndrome
• MONDO:0022321 ! 2-methylacetoacetyl coa thiolase deficiency
• MONDO:0022323 ! 2-hydroxyethyl methacrylate sensitization
• MONDO:0022326 ! 3 methylcrotonyl-coa carboxylase 1 deficiency
• MONDO:0022330 ! 4-hydroxyphenylacetic aciduria
• MONDO:0022333 ! 5-nucleotidase syndrome
• MONDO:0022337 ! AIDS dysmorphic syndrome
• MONDO:0022338 ! ALK+ histiocytosis
• MONDO:0022349 ! congenital absence of septum pellucidum
• MONDO:0022357 ! congenital acardia
• MONDO:0022380 ! acute lymphoblastic leukemia congenital sporadic aniridia
• MONDO:0022398 ! aglossia and situs inversus
• MONDO:0022401 ! agyria pachygyria polymicrogyria
• MONDO:0022402 ! agyria-pachygyria type 1
• MONDO:0022403 ! ahumada del castillo syndrome
• MONDO:0022406 ! aksu von stockhausen syndrome
• MONDO:0022412 ! albinism immunodeficiency
• MONDO:0022413 ! Albright-like syndrome
• MONDO:0022414 ! allain-babin-demarquez syndrome
• MONDO:0022417 ! alopecia congenita keratosis palmoplantaris
• MONDO:0022418 ! alopecia immunodeficiency
• MONDO:0022423 ! alpha-2 deficient collagen disease
• MONDO:0022424 ! alpha-mannosidosis type 1
• MONDO:0022425 ! alpha-thalassemia-abnormal morphogenesis
• MONDO:0022428 ! aluminium lung
• MONDO:0022432 ! alves castelo dos santos syndrome
• MONDO:0022434 ! amelia cleft lip palate hydrocephalus iris coloboma
• MONDO:0022444 ! amyloidosis bronchopulmonary
• MONDO:0022446 ! amyloidosis nodular localized cutaneous
• MONDO:0022448 ! amyoplasia mandibulofacial dysostosis
• MONDO:0022453 ! angiomyomatous hamartoma
• MONDO:0022454 ! angiosarcoma of the scalp
• MONDO:0022456 ! ankle defects short stature
• MONDO:0022457 ! ankyloblepharon filiforme imperforate anus
• MONDO:0022458 ! annular constricting bands
• MONDO:0022460 ! anophthalmia cleft lip palate hypothalamic disorder
• MONDO:0022461 ! anophthalmia cleft palate micrognathia
• MONDO:0022462 ! anophthalmia esophageal atresia cryptorchidism
• MONDO:0022463 ! anophthalmia megalocornea cardiopathy skeletal anomalies
• MONDO:0022464 ! anophthalmia microcephaly hypogonadism
• MONDO:0022465 ! anotia facial palsy cardiac defect
• MONDO:0022468 ! antigen-peptide-transporter 2 deficiency
• MONDO:0022469 ! aortic arches defect
• MONDO:0022470 ! aortic dissection lentiginosis
• MONDO:0022471 ! childhood aortic valve stenosis
• MONDO:0022481 ! APO A-i deficiency
• MONDO:0022482 ! apolipoprotein C 2i deficiency
• MONDO:0022495 ! arthritis short stature deafness
• MONDO:0022496 ! arthrogryposis iugr thoracic dystrophy
• MONDO:0022500 ! arthrogryposis multiplex congenita CNS calcification
• MONDO:0022504 ! arthrogryposis spinal muscular atrophy
• MONDO:0022509 ! asternia
• MONDO:0022510 ! atlanto-axial fusion
• MONDO:0022512 ! atrial septal defect coronary sinus
• MONDO:0022513 ! atrophoderma of Pierini and Pasini
• MONDO:0022518 ! autoimmune inner ear disease
• MONDO:0022519 ! autoimmune myocarditis
• MONDO:0022529 ! bk-virus nephropathy
• MONDO:0022545 ! barnicoat baraitser syndrome
• MONDO:0022546 ! basal cell nevus anodontia abnormal bone mineralization
• MONDO:0022551 ! basedow's coma
• MONDO:0022552 ! bazopoulou kyrkanidou syndrome
• MONDO:0022553 ! BD syndrome
• MONDO:0022555 ! beardwell syndrome
• MONDO:0022556 ! oculo-cerebral dysplasia
• MONDO:0022557 ! behrens baumann dust syndrome
• MONDO:0022559 ! benign angiitis of the central nervous system
• MONDO:0022560 ! benign metastasizing leiomyoma
• MONDO:0022566 ! BEST1 retinopathy
• MONDO:0022567 ! bhaskar jagannathan syndrome
• MONDO:0022568 ! bidirectional tachycardia
• MONDO:0022572 ! bilateral renal agenesis dominant type
• MONDO:0022573 ! biliary atresia intrahepatic non syndromic form
• MONDO:0022574 ! biliary atresia intrahepatic syndromic form
• MONDO:0022575 ! biliary hypoplasia
• MONDO:0022576 ! bilirubin induced brain injury in the newborn
• MONDO:0022577 ! billet bear syndrome
• MONDO:0022578 ! childhood bladder carcinoma
• MONDO:0022580 ! blepharo naso facial syndrome van maldergem type
• MONDO:0022586 ! bone dysplasia moore type
• MONDO:0022587 ! bone dysplasia corpus callosum agenesis
• MONDO:0022598 ! brachydactyly absence of distal phalanges
• MONDO:0022599 ! brachydactyly anonychia
• MONDO:0022602 ! brachydactyly small stature face anomalies
• MONDO:0022603 ! brachydactyly tibial hypoplasia
• MONDO:0022605 ! brachymetapody anodontia hypotrichosis albinoidism
• MONDO:0022606 ! branchial arch disease
• MONDO:0022607 ! extraovarian brenner tumor of the vagina
• MONDO:0022608 ! brittle bone syndrome lethal type
• MONDO:0022609 ! bronchial adenomas/carcinoids childhood
• MONDO:0022610 ! bronchiectasis oligospermia
• MONDO:0022611 ! brunoni syndrome
• MONDO:0022612 ! brunsting-perry syndrome
• MONDO:0022613 ! bruyn scheltens syndrome
• MONDO:0022615 ! burn goodship syndrome
• MONDO:0022618 ! burning mouth syndrome type 3
• MONDO:0022620 ! CD4 deficiency
• MONDO:0022622 ! CDG syndrome type 4
• MONDO:0022623 ! CDK4 linked melanoma
• MONDO:0022633 ! camptodactyly joint contractures and facial skeletal dysplasia
• MONDO:0022634 ! camptodactyly vertebral fusion
• MONDO:0022636 ! candida glabrata
• MONDO:0022639 ! cantu sanchez-corona garcia-cruz syndrome
• MONDO:0022642 ! childhood carcinoid tumor
• MONDO:0022643 ! carcinoma of the vocal tract
• MONDO:0022644 ! cardiac hydatid cysts with intracavitary expansion
• MONDO:0022645 ! cardioencephalomyopathy
• MONDO:0022646 ! cardiofacial syndrome short limbs
• MONDO:0022647 ! cardiomelic syndrome stratton koehler type
• MONDO:0022648 ! cardiomyopathy and deafness due to trna lysine gene mutation
• MONDO:0022650 ! cardiomyopathy diabetes deafness
• MONDO:0022651 ! cardiomyopathy dilated with conduction defect type 1
• MONDO:0022652 ! cardiomyopathy dilated with conduction defect type 2
• MONDO:0022653 ! cardiomyopathy due to anthracyclines
• MONDO:0022654 ! cardiomyopathy hypogonadism collagenoma syndrome
• MONDO:0022655 ! cardiomyopathy hypogonadism metabolic anomalies
• MONDO:0022656 ! cardiomyopathy spherocytosis
• MONDO:0022662 ! carpo tarsal osteolysis recessive
• MONDO:0022666 ! cassavism
• MONDO:0022672 ! autosomal dominant cataract
• MONDO:0022673 ! autosomal dominant non-nuclear cataract
• MONDO:0022675 ! cataract skeletal anomalies
• MONDO:0022676 ! cataract-glaucoma
• MONDO:0022682 ! cennamo gangemi syndrome
• MONDO:0022685 ! cerebellar agenesis
• MONDO:0022687 ! cerebellar degeneration
• MONDO:0022691 ! cerebello-olivary atrophy
• MONDO:0022693 ! cerebral calcification cerebellar hypoplasia
• MONDO:0022694 ! cerebral calcifications opalescent teeth phosphaturia
• MONDO:0022697 ! cerebral palsy athetoid
• MONDO:0022698 ! spastic diplegia cerebral palsy
• MONDO:0022699 ! cerebral palsy spastic hemiplegic
• MONDO:0022700 ! cerebral palsy spastic monoplegic
• MONDO:0022712 ! oculo digital syndrome
• MONDO:0022714 ! chester porphyria
• MONDO:0022715 ! Chiari malformation type 3
• MONDO:0022716 ! Chiari malformation type 4
• MONDO:0022723 ! chondrodysplasia
• MONDO:0022725 ! chondrodysplasia lethal recessive
• MONDO:0022728 ! chondrodysplasia punctata sheffield type
• MONDO:0022729 ! chondrodysplasia punctata with steroid sulfatase deficiency
• MONDO:0022732 ! chorea minor
• MONDO:0022733 ! choreoacanthocytosis amyotrophic
• MONDO:0022734 ! chorioretinopathy dominant form microcephaly
• MONDO:0022735 ! choroid plexus cyst
• MONDO:0022737 ! choroideremia hypopituitarism
• MONDO:0022739 ! christian demyer franken syndrome
• MONDO:0022740 ! christian johnson angenieta syndrome
• MONDO:0022746 ! chromosome 13p duplication
• MONDO:0022752 ! chromosome 16p13.3 deletion syndrome
• MONDO:0022754 ! chromosome 17 deletion
• MONDO:0022755 ! chromosome 18 mosaic monosomy
• MONDO:0022756 ! chromosome 1q deletion
• MONDO:0022757 ! chromosome 20 trisomy
• MONDO:0022758 ! chromosome 22, monosome mosaic
• MONDO:0022759 ! trisomy 22
• MONDO:0022760 ! chromosome 22q deletion
• MONDO:0022761 ! chromosome 3 duplication syndrome
• MONDO:0022762 ! chromosome 4 short arm deletion
• MONDO:0022765 ! chronic demyelinizing neuropathy with igm monoclonal
• MONDO:0022768 ! chronic polyradiculoneuritis
• MONDO:0022769 ! ciliary dyskinesia-bronchiectasis
• MONDO:0022770 ! circumscribed cutaneous aplasia of the vertex
• MONDO:0022771 ! circumscribed disseminated keratosis jadassohn lew type
• MONDO:0022772 ! classic kaposi sarcoma
• MONDO:0022775 ! cleft lip and palate malrotation cardiopathy
• MONDO:0022776 ! cleft lip and/or palate with mucous cysts of lower
• MONDO:0022777 ! cleft lip palate dysmorphism kumar type
• MONDO:0022778 ! cleft lip palate mental retardation corneal opacity
• MONDO:0022779 ! cleft lip palate oligodontia syndactyly pili torti
• MONDO:0022780 ! cleft lip palate pituitary deficiency
• MONDO:0022781 ! cleft lip palate-tetraphocomelia
• MONDO:0022782 ! cleft lower lip cleft lateral canthi chorioretinal
• MONDO:0022785 ! cleft palate cardiac defect ectrodactyly
• MONDO:0022786 ! cleft palate colobomata radial synostosis deafness
• MONDO:0022787 ! cleft palate heart disease polydactyly absent tibia
• MONDO:0022790 ! cleft tongue
• MONDO:0022791 ! coarse face hypotonia constipation
• MONDO:0022792 ! coccygodynia
• MONDO:0022795 ! deficiency of coenzyme q cytochrome c reductase
• MONDO:0022798 ! cohen lockood wyborney syndrome
• MONDO:0022799 ! cold urticaria
• MONDO:0022800 ! collagenopathy type 2 alpha 1
• MONDO:0022802 ! collins sakati syndrome
• MONDO:0022803 ! coloboma porencephaly hydronephrosis
• MONDO:0022804 ! colobomata unilobar lung heart defect
• MONDO:0022805 ! colonic malakoplakia
• MONDO:0022808 ! colpocephaly
• MONDO:0022809 ! colver steer godman syndrome
• MONDO:0022810 ! combarros calleja leno syndrome
• MONDO:0022812 ! complement receptor deficiency
• MONDO:0022815 ! congenital absence of the sternocleidomastoid muscle
• MONDO:0022817 ! congenital amputation
• MONDO:0022818 ! congenital aneurysms of the great vessels
• MONDO:0022819 ! congenital arteriovenous shunt
• MONDO:0022820 ! congenital articular rigidity
• MONDO:0022821 ! congenital benign spinal muscular atrophy dominant
• MONDO:0022822 ! congenital cardiovascular shunt
• MONDO:0022823 ! congenital contractures
• MONDO:0022824 ! congenital craniosynostosis maternal hyperthyroiditis
• MONDO:0022825 ! congenital cystic eye
• MONDO:0022826 ! congenital cystic eye multiple ocular and intracranial anomalies
• MONDO:0022831 ! congenital heart disease ptosis hypodontia craniostosis
• MONDO:0022832 ! congenital heart disease radio ulnar synostosis mental retardation
• MONDO:0022839 ! congenital human immunodeficiency virus
• MONDO:0022841 ! congenital hypotrichosis milia
• MONDO:0022843 ! congenital mumps
• MONDO:0022846 ! congenital nonhemolytic jaundice
• MONDO:0022849 ! congenital stenosis of cervical medullary canal
• MONDO:0022850 ! congenital sucrose isomaltose malabsorption
• MONDO:0022851 ! Dennis-Fairhurst-Moore syndrome
• MONDO:0022854 ! congenital unilateral pulmonary hypoplasia
• MONDO:0022855 ! congenital vagal hyperreflexivity
• MONDO:0022856 ! conjunctivitis with pseudomembrane
• MONDO:0022857 ! continuous muscle fiber activity hereditary
• MONDO:0022858 ! continuous spike-wave during slow sleep syndrome
• MONDO:0022859 ! cor biloculare
• MONDO:0022862 ! cormier rustin munnich syndrome
• MONDO:0022863 ! corneal crystals myopathy neuropathy
• MONDO:0022865 ! corneal dystrophy ichthyosis microcephaly mental retardation
• MONDO:0022866 ! corneal dystrophy pigmentary anomaly malabsorption
• MONDO:0022869 ! coronary arteries congenital malformation
• MONDO:0022871 ! corpus callosum agenesis of blepharophimosis robin type
• MONDO:0022872 ! corpus callosum dysgenesis x-linked recessive
• MONDO:0022873 ! corpus callosum dysgenesis cleft spasm
• MONDO:0022874 ! corpus callosum dysgenesis hypopituitarism
• MONDO:0022875 ! cortada koussef matsumoto syndrome
• MONDO:0022876 ! cortes lacassie syndrome
• MONDO:0022880 ! corticobasal degeneration
• MONDO:0022883 ! craniofacial and skeletal defects
• MONDO:0022884 ! craniofacial dysostosis arthrogryposis progeroid appearence
• MONDO:0022885 ! craniofacial dystonia
• MONDO:0022887 ! craniofrontonasal syndrome teebi type
• MONDO:0022888 ! craniostenosis cataract
• MONDO:0022889 ! craniostenosis with congenital heart disease mental retardation
• MONDO:0022890 ! craniosynostosis fontaine type
• MONDO:0022891 ! craniosynostosis maroteaux fonfria type
• MONDO:0022892 ! craniosynostosis alopecia brain defect
• MONDO:0022893 ! craniosynostosis arthrogryposis cleft palate
• MONDO:0022894 ! craniosynostosis autosomal dominant
• MONDO:0022895 ! craniosynostosis cleft lip palate arthrogryposis
• MONDO:0022896 ! craniosynostosis contractures cleft
• MONDO:0022897 ! craniosynostosis exostoses nevus epibulbar dermoid
• MONDO:0022898 ! craniosynostosis mental retardation heart defects
• MONDO:0022899 ! crawfurd syndrome
• MONDO:0022900 ! athyreotic congenital hypothyroidism
• MONDO:0022901 ! crohn's disease of the esophagus
• MONDO:0022904 ! cryofibrinogenemia
• MONDO:0022907 ! cutaneous sclerosis
• MONDO:0022908 ! cutis gyratum acanthosis nigricans craniosynostosis
• MONDO:0022909 ! cutis laxa osteoporosis
• MONDO:0022912 ! cutis verticis gyrata mental deficiency
• MONDO:0022913 ! cutler bass romshe syndrome
• MONDO:0022916 ! cystic hygroma lethal cleft palate
• MONDO:0022918 ! cytokine deficiency
• MONDO:0022919 ! cytokine receptor deficiency
• MONDO:0022926 ! daentl towsend siegel syndrome
• MONDO:0022930 ! dandy-walker malformation with nasopharyngeal teratoma and diaphragmatic hernia
• MONDO:0022932 ! Davenport-Donlan syndrome
• MONDO:0022934 ! davis lafer syndrome
• MONDO:0022936 ! de hauwere leroy adriaenssens syndrome
• MONDO:0022937 ! deafness conductive stapedial ear malformation facial palsy
• MONDO:0022938 ! deafness goiter stippled epiphyses
• MONDO:0022939 ! deafness hyperuricemia neurologic ataxia
• MONDO:0022940 ! deafness hyperuricemia neurologic ataxia
• MONDO:0022941 ! deafness hypospadias metacarpal and metatarsal syndrome
• MONDO:0022942 ! deafness mesenteric diverticula of small bowel neuropathy
• MONDO:0022945 ! deafness peripheral neuropathy arterial disease
• MONDO:0022946 ! deafness progressive cataract autosomal dominant
• MONDO:0022948 ! deal barratt dillon syndrome
• MONDO:0022949 ! defective apolipoprotein b-100
• MONDO:0022953 ! delta-1-pyrroline-5-carboxylate dehydrogenase deficiency
• MONDO:0022960 ! dermatocardioskeletal syndrome boronne type
• MONDO:0022963 ! desmoplastic infantile astrocytoma
• MONDO:0022965 ! desmoplastic infantile ganglioglioma
• MONDO:0022968 ! dextrocardia with situs inversus
• MONDO:0022971 ! diabetes persistent mullerian ducts
• MONDO:0022972 ! diabetic mastopathy
• MONDO:0022975 ! diaphragmatic agenesis radial aplasia omphalocele
• MONDO:0022977 ! diaphragmatic hernia exomphalos corpus callosum agenesis
• MONDO:0022978 ! diaphragmatic hernia upper limb defects
• MONDO:0022981 ! die smulders droog van dijk syndrome
• MONDO:0022982 ! die smulders vles fryns syndrome
• MONDO:0022983 ! dieterich's disease
• MONDO:0022985 ! diffuse cavernous hemangioma of the rectum
• MONDO:0022986 ! diffuse idiopathic pulmonary neuroendocrine cell hyperplasia
• MONDO:0022989 ! diomedi bernardi placidi syndrome
• MONDO:0022990 ! diphallus rachischisis imperforate anus
• MONDO:0022991 ! diploid-triploid mosaicism
• MONDO:0022993 ! dipsogenic diabetes insipidus
• MONDO:0022998 ! distal arthrogryposis moore weaver type
• MONDO:0022999 ! distichiasis heart congenital anomalies
• MONDO:0023000 ! dobrow syndrome
• MONDO:0023002 ! double discordia
• MONDO:0023003 ! double fingernail of fifth finger
• MONDO:0023005 ! double uterus-hemivagina-renal agenesis
• MONDO:0023006 ! doxorubicin induced cardiomyopathy
• MONDO:0023007 ! drachtman weinblatt sitarz syndrome
• MONDO:0023008 ! drachtman weinblatt sitarz syndrome
• MONDO:0023013 ! duker weiss siber syndrome
• MONDO:0023015 ! duodenal atresia tetralogy of fallot
• MONDO:0023016 ! duplication of leg mirror foot
• MONDO:0023017 ! duplication of the thumb unilateral biphalangeal
• MONDO:0023018 ! dupont sellier chochillon syndrome
• MONDO:0023019 ! dwarfism bluish sclerae
• MONDO:0023020 ! dwarfism deafness retinitis pigmentosa
• MONDO:0023021 ! dwarfism lethal type advanced bone age
• MONDO:0023022 ! dwarfism thin bones multiple fractures
• MONDO:0023030 ! dysmorphism cleft palate loose skin
• MONDO:0023031 ! dysostosis acral with facial and genital abnormalities
• MONDO:0023035 ! eagle syndrome
• MONDO:0023037 ! elongated styloid process syndrome
• MONDO:0023038 ! eccentrochondrodysplasia
• MONDO:0023039 ! eccrine mucinous carcinoma
• MONDO:0023040 ! ectodermal dysplasia bartalos type
• MONDO:0023041 ! ectodermal dysplasia berlin type
• MONDO:0023042 ! ectodermal dysplasia margarita type
• MONDO:0023043 ! ectodermal dysplasia alopecia preaxial polydactyly
• MONDO:0023045 ! ectodermal dysplasia arthrogryposis diabetes mellitus
• MONDO:0023046 ! ectodermal dysplasia blindness
• MONDO:0023048 ! ectodermal dysplasia neurosensory deafness
• MONDO:0023050 ! ectrodactyly cardiopathy dysmorphism
• MONDO:0023052 ! ectrodactyly polydactyly
• MONDO:0023059 ! elliott ludman teebi syndrome
• MONDO:0023061 ! enamel hypoplasia cataract hydrocephaly
• MONDO:0023062 ! encephalocele anencephaly
• MONDO:0023065 ! encephalopathy recurrent of childhood
• MONDO:0023066 ! enchondromatosis dwarfism deafness
• MONDO:0023067 ! endemic kaposi sarcoma
• MONDO:0023068 ! engelhard yatziv syndrome
• MONDO:0023069 ! enlarged vestibular aqueduct syndrome
• MONDO:0023070 ! enteropathica
• MONDO:0023071 ! enterovirus antenatal infection
• MONDO:0023072 ! envenomization by bothrops lanceolatus
• MONDO:0023073 ! eosinophilic cryptitis
• MONDO:0023076 ! eosinophilic pustular folliculitis
• MONDO:0023079 ! epidermal nevus vitamin D resistant rickets
• MONDO:0023083 ! epimetaphyseal dysplasia cataract
• MONDO:0023084 ! epiphyseal dysplasia dysmorphism camptodactyly
• MONDO:0023089 ! erythroplakia
• MONDO:0023091 ! esophageal atresia coloboma talipes
• MONDO:0023093 ! exertional headache
• MONDO:0023094 ! exogenous ochronosis
• MONDO:0023097 ! exostoses anetodermia brachydactyly type E
• MONDO:0023098 ! extrasystoles short stature hyperpigmentation microcephaly
• MONDO:0023099 ! FRAXD syndrome
• MONDO:0023100 ! facial clefting corpus callosum agenesis
• MONDO:0023101 ! facio digito genital syndrome recessive form
• MONDO:0023102 ! facio skeletal genital syndrome rippberger type
• MONDO:0023106 ! fairbank disease
• MONDO:0023111 ! familial capillaro-venous leptomeningeal angiomatosis
• MONDO:0023113 ! familial colorectal cancer
• MONDO:0023119 ! familial myelofibrosis
• MONDO:0023121 ! familial partial paralysis
• MONDO:0023122 ! familial prostate cancer
• MONDO:0023124 ! familial pulmonary arterial hypertension leucopenia and atrial septal defect
• MONDO:0023129 ! fara chlupackova syndrome
• MONDO:0023133 ! faye-petersen ward carey syndrome
• MONDO:0023134 ! febrile ulceronecrotic mucha-habermann disease
• MONDO:0023137 ! feigenbaum bergeron syndrome
• MONDO:0023138 ! feingold trainer syndrome
• MONDO:0023140 ! fenton wilkinson toselano syndrome
• MONDO:0023141 ! antihypertensive drugs antenatal exposure syndrome
• MONDO:0023142 ! fetal brain disruption sequence
• MONDO:0023143 ! fetal enterovirus syndrome
• MONDO:0023147 ! fetal parainfluenza virus type 3 syndrome
• MONDO:0023148 ! fetal phenothiazine syndrome
• MONDO:0023152 ! fibrocartilaginous embolism
• MONDO:0023154 ! fibromatosis multiple non ossifying
• MONDO:0023155 ! fibula aplasia complex brachydactyly
• MONDO:0023157 ! fibular hypoplasia scapulo pelvic dysplasia absent
• MONDO:0023158 ! fitz-hugh-curtis syndrome
• MONDO:0023165 ! florid cystic endosalpingiosis of the uterus
• MONDO:0023167 ! focal alopecia congenital megalencephaly
• MONDO:0023170 ! focal or multifocal malformations in neuronal migration
• MONDO:0023171 ! foix chavany marie syndrome
• MONDO:0023174 ! follicular lymphoreticuloma
• MONDO:0023175 ! fontaine farriaux blanckaert syndrome
• MONDO:0023176 ! formaldehyde poisoning
• MONDO:0023178 ! fragile x syndrome type 1
• MONDO:0023179 ! fragile x syndrome type 2
• MONDO:0023180 ! fragile x syndrome type 3
• MONDO:0023182 ! franceschini vardeu guala syndrome
• MONDO:0023186 ! fraser jequier chen syndrome
• MONDO:0023188 ! freiberg's disease
• MONDO:0023191 ! freire-maia odontotrichomelic syndrome
• MONDO:0023193 ! friedman goodman syndrome
• MONDO:0023194 ! frints de smet fabry fryns syndrome
• MONDO:0023196 ! fronto nasal malformation cloacal exstrophy
• MONDO:0023197 ! frontonasal dysplasia klippel feil syndrome
• MONDO:0023199 ! frontonasal dysplasia phocomelic upper limbs
• MONDO:0023200 ! fryns fabry remans syndrome
• MONDO:0023201 ! fryns smeets thiry syndrome
• MONDO:0023203 ! fuchs atrophia gyrata chorioideae et retinae
• MONDO:0023204 ! fukuda miyanomae nakata syndrome
• MONDO:0023206 ! functional pancreatic neuroendocrine tumor
• MONDO:0023208 ! fuqua berkovitz syndrome
• MONDO:0023209 ! galactorrhoea-hyperprolactinaemia
• MONDO:0023212 ! garret tripp syndrome
• MONDO:0023214 ! gas bloat syndrome
• MONDO:0023217 ! gastro-enteropancreatic neuroendocrine tumor
• MONDO:0023221 ! gaucher ichthyosis restrictive dermopathy
• MONDO:0023224 ! inherited reflex epilepsy
• MONDO:0023226 ! gershinibaruch leibo syndrome
• MONDO:0023227 ! gestational diabetes insipidus
• MONDO:0023230 ! ghose sachdev kumar syndrome
• MONDO:0023232 ! giant cell myocarditis
• MONDO:0023235 ! giant congenital nevus
• MONDO:0023238 ! giant mammary hamartoma
• MONDO:0023240 ! gigantism advanced bone age hoarse cry
• MONDO:0023243 ! glass-chapman-hockley syndrome
• MONDO:0023250 ! global disaccharide intolerance
• MONDO:0023255 ! glossopalatine ankylosis micrognathia ear anomalies
• MONDO:0023258 ! glucose-6-phosphate translocase deficiency
• MONDO:0023263 ! glyceraldehyde-3-phosphate dehydrogenase deficiency
• MONDO:0023267 ! goldstein hutt syndrome
• MONDO:0023272 ! goniodysgenesis mental retardation short stature
• MONDO:0023275 ! graham boyle troxell syndrome
• MONDO:0023282 ! granulomatous hypophysitis
• MONDO:0023283 ! ovarian granulosa cell tumor
• MONDO:0023286 ! graphite pneumoconiosis
• MONDO:0023288 ! green sandford davison syndrome
• MONDO:0023290 ! grix blankenship peterson syndrome
• MONDO:0023297 ! guttate psoriasis
• MONDO:0023303 ! Hamanishi-Ueba-Tsuji syndrome
• MONDO:0023305 ! heavy metal poisoning
• MONDO:0023310 ! hemiplegic migraine
• MONDO:0023368 ! Ho-Kaufman-McAlister syndrome
• MONDO:0023369 ! disease of facial skeleton
• MONDO:0023370 ! neoplastic disease
• MONDO:0023419 ! hyperprolinemia
• MONDO:0023472 ! chondrodysplasia situs inversus imperforate anus polydactyly
• MONDO:0023483 ! infectious myositis
• MONDO:0023510 ! Jaffer-Beighton syndrome
• MONDO:0023513 ! Jeune syndrome situs inversus
• MONDO:0023521 ! Judge Misch Wright syndrome
• MONDO:0023528 ! KSHV inflammatory cytokine syndrome
• MONDO:0023530 ! kallikrein hypertension
• MONDO:0023538 ! Kaplowitz-Bodurtha syndrome
• MONDO:0023540 ! Kashani-Strom-Utley syndrome
• MONDO:0023541 ! Kasznica-Carlson-Coppedge syndrome
• MONDO:0023543 ! Katsantoni-Papadakou-Lagoyanni syndrome
• MONDO:0023558 ! Kocher-Debre-Semelaigne syndrome
• MONDO:0023561 ! koone rizzo elias syndrome
• MONDO:0023563 ! Kotzot-Richter syndrome
• MONDO:0023567 ! kozlowski Brown Hardwick syndrome
• MONDO:0023569 ! Kozlowski Ouvrier syndrome
• MONDO:0023571 ! Kozlowski Rafinski Klicharska syndrome
• MONDO:0023573 ! Kozlowski Warren Fisher syndrome
• MONDO:0023575 ! Krauss Herman Holmes syndrome
• MONDO:0023577 ! Krieble Bixler syndrome
• MONDO:0023579 ! Kuster Majewski Hammerstein syndrome
• MONDO:0023581 ! Kuster syndrome
• MONDO:0023597 ! laryngeal papillomatosis
• MONDO:0023601 ! non-classic congenital adrenal hyperplasia
• MONDO:0023605 ! Laugier-Hunziker syndrome
• MONDO:0023607 ! laurence prosser rocker syndrome
• MONDO:0023609 ! le Marec Bracq Picaud syndrome
• MONDO:0023616 ! familial leiomyomatosis
• MONDO:0023619 ! lentigo maligna melanoma
• MONDO:0023628 ! levator syndrome
• MONDO:0023644 ! lip and oral cavity carcinoma
• MONDO:0023646 ! lipodermatosclerosis
• MONDO:0023650 ! littoral cell angioma of the spleen
• MONDO:0023663 ! macrocephaly mesodermal hamartoma spectrum
• MONDO:0023691 ! maple syrup urine disease type 1a
• MONDO:0023692 ! maple syrup urine disease type 1b
• MONDO:0023693 ! maple syrup urine disease type 2
• MONDO:0023696 ! Marinesco-Sjogren-like syndrome
• MONDO:0023699 ! Maroteaux Fonfria syndrome
• MONDO:0023704 ! Martinez Monasterio Pinheiro syndrome
• MONDO:0023726 ! mediastinal yolk sac tumor
• MONDO:0023757 ! meralgia paresthetica
• MONDO:0023809 ! Milner-Khallouf-Gibson syndrome
• MONDO:0023820 ! moebius axonal neuropathy hypogonadism
• MONDO:0023833 ! multifocal choroiditis
• MONDO:0024234 ! seckel like syndrome majoor-krakauer type
• MONDO:0024235 ! Brenner tumor
• MONDO:0024236 ! degenerative disorder
• MONDO:0024237 ! inherited neurodegenerative disorder
• MONDO:0024238 ! cerebral degeneration
• MONDO:0024239 ! congenital anomaly of cardiovascular system
• MONDO:0024240 ! eccrine carcinoma
• MONDO:0024245 ! ductal eccrine adenocarcinoma
• MONDO:0024246 ! syringofibroadenoma
• MONDO:0024247 ! benign eccrine neoplasm
• MONDO:0024249 ! pityriasis lichenoides
• MONDO:0024250 ! acute lichenoid pityriasis
• MONDO:0024251 ! Minamata disease
• MONDO:0024252 ! global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome
• MONDO:0024253 ! early-onset epilepsy-intellectual disability-brain anomalies syndrome
• MONDO:0024254 ! vibratory angioedema
• MONDO:0024255 ! genetic skin disease
• MONDO:0024257 ! genetic motor neuron disease
• MONDO:0024262 ! massive neonatal aspiration syndrome
• MONDO:0024263 ! neonatal aspiration syndrome
• MONDO:0024264 ! hypothyroidism, congenital, nongoitrous, 2
• MONDO:0024265 ! Duane syndrome type 1
• MONDO:0024266 ! patent ductus arteriosus 3
• MONDO:0024267 ! encephalitis lethargica