• • disease
    • human disease
      • acute disease
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      • auditory system disorder
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      • breast disorder
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      • cancer or benign tumor
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      • cardiovascular disorder
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      • chromosomal disorder
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      • connective tissue disorder
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      • digestive system disorder
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      • disease related to transplantation
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      • disorder of development or morphogenesis
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      • disorder of orbital region
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      • disorder of visual system
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      • endocrine system disorder
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      • hematologic disorder
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      • hereditary disease
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      • iatrogenic disease
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      • idiopathic disease
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      • immune system disorder
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      • infectious disease
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      • inflammatory disease
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      • integumentary system disorder
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      • metabolic disease
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      • mitochondrial disease
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      • mouth disorder
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      • musculoskeletal system disorder
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      • nervous system disorder
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      • nutritional disorder
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      • obstetric disorder
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      • occupational disorder
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      • otorhinolaryngologic disease
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      • perinatal disease
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      • poisoning
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      • post-bacterial disorder
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      • post-COVID-19 disorder
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      • post-infectious disorder
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      • post-viral disorder
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      • psychiatric disorder
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      • radiation-induced disorder
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      • reproductive system disorder
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      • respiratory system disorder
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      • syndromic disease
        • achalasia-alacrima syndrome
        • acute coronary syndrome
        • Adams-Stokes syndrome
        • agnathia-microstomia-synotia
        • agyria pachygyria polymicrogyria
        • agyria-pachygyria type 1
        • Albright-like syndrome
        • Alkuraya-Kucinskas syndrome
        • ankle defects short stature
        • anotia facial palsy cardiac defect
        • arthrogryposis spinal muscular atrophy
        • Axenfeld-Rieger syndrome
        • B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome
        • Banti syndrome
        • Bardet-Biedl syndrome
        • Barnicoat Baraitser syndrome
        • Behcet disease
        • Bonnevie-Ullrich syndrome
        • branchio-oto-renal syndrome
        • camptodactyly joint contractures and facial skeletal dysplasia
        • cardiofacial syndrome short limbs
        • cardiomyopathy and deafness due to tRNA lysine gene mutation
        • Cartwright Nelson Fryns syndrome
        • cataract-nephropathy-encephalopathy syndrome
        • cerebellar agenesis
        • Charles bonnet syndrome
        • choreoacanthocytosis amyotrophic
        • Christianson syndrome
        • chromosome 18q deletion syndrome
        • cleft lip and/or palate with mucous cysts of lower
        • cleft lip palate dysmorphism kumar type
        • cleft lip/palate-deafness-sacral lipoma syndrome
        • cleidocranial dysplasia 1
        • Combarros Calleja Leno syndrome
        • complement receptor deficiency
        • congenital cardiovascular shunt
        • congenital contractures
        • congenital heart disease radio ulnar synostosis intellectual disability
        • cormier rustin munnich syndrome
        • corneal crystals myopathy neuropathy
        • corneal dystrophy ichthyosis microcephaly intellectual disability
        • corneal dystrophy pigmentary anomaly malabsorption
        • corpus callosum dysgenesis cleft spasm
        • corpus callosum dysgenesis hypopituitarism
        • cortada Koussef Matsumoto syndrome
        • Cortes Lacassie syndrome
        • Crandall syndrome
        • craniofacial dysostosis arthrogryposis progeroid appearence
        • craniofrontonasal syndrome Teebi type
        • craniostenosis with congenital heart disease intellectual disability
        • developmental and speech delay due to SOX5 deficiency
        • diaphragmatic hernia exomphalos corpus callosum agenesis
        • Duane retraction syndrome
        • Duker-Weiss-Siber syndrome
        • dupont sellier chochillon syndrome
        • ectodermal dysplasia syndrome
          • Ackerman syndrome
          • acrofacial dysostosis, Weyers type
          • alves Castelo dos Santos syndrome
          • amelocerebrohypohidrotic syndrome
          • ameloonychohypohidrotic syndrome
          • anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome
          • Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
            • Rosselli-Gulienetti syndrome
          • anonychia with flexural pigmentation
          • AREDYLD syndrome
          • arthrogryposis-ectodermal dysplasia-other anomalies syndrome
          • autosomal dominant palmoplantar keratoderma and congenital alopecia
          • autosomal dominant trichoodontoonychodysplasia-syndactyly
          • autosomal recessive palmoplantar keratoderma and congenital alopecia
          • Barber-Say syndrome
          • Bartsocas-Papas syndrome 1
          • blepharocheilodontic syndrome
            • blepharocheilodontic syndrome 1
            • blepharocheilodontic syndrome 2
            • Martinez Monasterio Pinheiro syndrome
          • Brunoni syndrome
          • Böök syndrome
          • cardiofaciocutaneous syndrome
            • cardiofaciocutaneous syndrome 1
            • cardiofaciocutaneous syndrome 2
            • cardiofaciocutaneous syndrome 3
            • cardiofaciocutaneous syndrome 4
          • cataract-hypertrichosis-intellectual disability syndrome
          • CHIME syndrome
          • chondroectodermal dysplasia with night blindness
          • choroidal atrophy-alopecia syndrome
          • cleft lip/palate-ectodermal dysplasia syndrome
          • Clouston syndrome
          • conductive deafness-ptosis-skeletal anomalies syndrome
          • congenital hypotrichosis with juvenile macular dystrophy
          • contractures-ectodermal dysplasia-cleft lip/palate syndrome
          • cranioectodermal dysplasia
            • cranioectodermal dysplasia 1
            • cranioectodermal dysplasia 2
            • cranioectodermal dysplasia 3
            • cranioectodermal dysplasia 4
            • short-rib thoracic dysplasia 16 with or without polydactyly
          • Cronkhite-Canada syndrome
          • Curly hair - acral keratoderma - caries syndrome
          • deafness-onychodystrophy syndrome
            • autosomal dominant deafness - onychodystrophy syndrome
            • DOORS syndrome
          • dermatoosteolysis, Kirghizian type
          • dermatopathia pigmentosa reticularis
          • dermo-odonto dysplasia
          • dermotrichic syndrome
          • Dubowitz syndrome
          • dyskeratosis congenita
            • autosomal recessive dyskeratosis congenita 4
            • DKC1-related disorder
            • dyskeratosis congenita, autosomal dominant 1
            • dyskeratosis congenita, autosomal dominant 2
            • dyskeratosis congenita, autosomal dominant 3
            • dyskeratosis congenita, autosomal dominant 4
            • dyskeratosis congenita, autosomal dominant 6
            • dyskeratosis congenita, autosomal recessive 1
            • dyskeratosis congenita, autosomal recessive 2
            • dyskeratosis congenita, autosomal recessive 3
            • dyskeratosis congenita, autosomal recessive 5
            • dyskeratosis congenita, autosomal recessive 6
            • dyskeratosis congenita, autosomal recessive 7
            • dyskeratosis congenita, autosomal recessive 8
            • dyskeratosis congenita, digenic
            • Revesz syndrome
          • ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type
          • ectodermal dysplasia 13, hair/tooth type
          • ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis
          • ectodermal dysplasia 15, hypohidrotic/hair type
          • ectodermal dysplasia alopecia preaxial polydactyly
          • ectodermal dysplasia arthrogryposis diabetes mellitus
          • ectodermal dysplasia Berlin type
          • ectodermal dysplasia blindness
          • ectodermal dysplasia margarita type
          • ectodermal dysplasia neurosensory deafness
          • ectodermal dysplasia with natal teeth, Turnpenny type
          • ectodermal dysplasia WNT10A related
            • odonto-onycho-dermal dysplasia
            • SchC6pf-Schulz-Passarge syndrome
            • tooth agenesis, selective, 4
          • ectodermal dysplasia, trichoodontoonychial type
          • ectodermal dysplasia-blindness syndrome
          • ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome
          • ectodermal dysplasia-sensorineural deafness syndrome
          • ectodermal dysplasia-syndactyly syndrome
            • ectodermal dysplasia-cutaneous syndactyly syndrome
            • ectodermal dysplasia-syndactyly syndrome 1
          • EEC syndrome and related syndrome
            • ADULT syndrome
            • EEC syndrome
            • limb-mammary syndrome
          • EEM syndrome
          • Ellis-van Creveld syndrome
            • Jeune syndrome situs inversus
          • epidermolysis bullosa simplex due to plakophilin deficiency
          • focal facial dermal dysplasia
            • focal facial dermal dysplasia type I
            • focal facial dermal dysplasia type III
            • focal facial dermal dysplasia type IV
          • Fontaine progeroid syndrome
          • gingival fibromatosis-hypertrichosis syndrome
          • hidrotic ectodermal dysplasia, Christianson-Fourie type
          • hidrotic ectodermal dysplasia, Halal type
          • hypertrichosis cubiti-short stature syndrome
          • hypertrichosis lanuginosa congenita
            • Ambras type hypertrichosis universalis congenita
            • X-linked congenital generalized hypertrichosis
          • hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
          • hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
          • incontinentia pigmenti
          • Ito hypomelanosis
          • jones hersh yusk syndrome
          • KID syndrome
            • autosomal dominant keratitis-ichthyosis-hearing loss syndrome
            • ichthyosiform erythroderma, corneal involvement, and hearing loss
            • ichthyosis, hystrix-like, with hearing loss
          • Marshall syndrome
          • Naegeli-Franceschetti-Jadassohn syndrome
          • nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome
          • oculodentodigital dysplasia
            • oculodentodigital dysplasia, autosomal recessive
          • oculoosteocutaneous syndrome
          • oculotrichodysplasia
          • odonto-onycho dysplasia-alopecia syndrome
          • odonto-tricho-ungual-digito-palmar syndrome
          • Papillon-Lefevre disease
          • pilodental dysplasia-refractive errors syndrome
          • pure hair and nail ectodermal dysplasia
            • ectodermal dysplasia 4, hair/nail type
            • ectodermal dysplasia 6, hair/nail type
            • ectodermal dysplasia 7, hair/nail type
            • ectodermal dysplasia 9, hair/nail type
          • Rapp-Hodgkin syndrome
          • scalp-ear-nipple syndrome
          • Schinzel-Giedion syndrome
          • Stern-Lubinsky-Durrie syndrome
          • taurodontia-absent teeth-sparse hair syndrome
          • Teebi-Shaltout syndrome
          • tooth and nail syndrome
          • Toriello-Lacassie-Droste syndrome
          • tricho-dento-osseous syndrome
          • tricho-oculo-dermo-vertebral syndrome
          • trichodental syndrome
          • trichodermodysplasia-dental alterations syndrome
          • trichomegaly-retina pigmentary degeneration-dwarfism syndrome
          • trichoodontoonychial dysplasia
          • trichorhinophalangeal syndrome
            • trichorhinophalangeal syndrome type I or III
            • trichorhinophalangeal syndrome type II
          • trichothiodystrophy
            • photosensitive trichothiodystrophy
            • trichothiodystrophy 4, nonphotosensitive
            • trichothiodystrophy 5, nonphotosensitive
            • trichothiodystrophy 6, nonphotosensitive
            • trichothiodystrophy 7, nonphotosensitive
            • trichothiodystrophy 8, nonphotosensitive
            • trichothiodystrophy 9, nonphotosensitive
        • engelhard yatziv syndrome
        • enlarged vestibular aqueduct syndrome
        • eosinophilic granulomatosis with polyangiitis
        • epidermal nevus vitamin D resistant rickets
        • epiphyseal dysplasia-hearing loss-dysmorphism syndrome
        • fibular hypoplasia scapulo pelvic dysplasia absent
        • Fitz-Hugh-Curtis syndrome
        • Gilbert syndrome
        • hemophagocytic syndrome
        • hypertrichotic osteochondrodysplasia Cantu type
        • hypoparathyroidism-deafness-renal disease syndrome
        • hypotrichosis-deafness syndrome
        • KINSSHIP syndrome
        • Koone-Rizzo-Elias syndrome
        • Landau-Kleffner syndrome
        • lateral medullary syndrome
        • methimazole embryofetopathy
        • microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome
        • multiple organ dysfunction syndrome
        • nephrogenic diabetes insipidus-intracranial calcification syndrome
        • Parinaud syndrome
        • parkinsonism-dystonia, infantile
        • pentasomy X
        • persian gulf syndrome
        • piriformis syndrome
        • pituitary stalk interruption syndrome
        • podder-tolmie syndrome
        • posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome
        • primary hypomagnesemia-generalized seizures-intellectual disability-obesity syndrome
        • progressive encephalomyelitis with rigidity
        • renal cysts and diabetes syndrome
        • richieri-costa guion-almeida cohen syndrome
        • Rubinstein Taybi like syndrome
        • SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome
        • shoulder and girdle defects-familial intellectual disability syndrome
        • Stankiewicz-Isidor syndrome
        • stiff-person syndrome
        • syndromic congenital sodium diarrhea
        • syndromic dyslipidemia
        • syndromic hyperopia
        • tubular renal disease-cardiomyopathy syndrome
        • Wissler syndrome
        • X-linked mandibulofacial dysostosis
        • Yunis-Varon syndrome
      • ulcer disease
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      • upper digestive tract disorder
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      • urinary system disorder
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    • non-human animal disease
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  • injury
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