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disease has basis in
- classic congenital mesoblastic nephroma
- Leber congenital amaurosis
- congenital malabsorptive diarrhea 4
- congenital bile acid synthesis defect 2
- primary congenital glaucoma
- congenital muscular dystrophy-dystroglycanopathy type A12
- congenital muscular dystrophy-dystroglycanopathy type A5
- congenital myasthenic syndrome 14
- severe congenital neutropenia 2
- congenital hereditary endothelial dystrophy of cornea
- nonsyndromic congenital nail disorder 9
- congenital myasthenic syndrome 21
- congenital nongoitrous hypothyroidism 7
- autosomal recessive congenital ichthyosis 6
- congenital nongoitrous hypothyroidism 6
- congenital disorder of glycosylation Ih
- congenital muscular dystrophy-dystroglycanopathy type A6
- congenital disorder of glycosylation Iq
- congenital dyserythropoietic anemia type Ia
- congenital hypogammaglobulinemia
- congenital myasthenic syndrome 1A
- autosomal recessive congenital bilateral absence of vas deferens
- severe congenital neutropenia 3
- Fukuyama congenital muscular dystrophy
- congenital diaphragmatic hernia
- congenital myasthenic syndrome 13
- Compton-North congenital myopathy
- autosomal recessive congenital ichthyosis 2
- Leber congenital amaurosis 10
- autosomal recessive congenital ichthyosis 1
- congenital disorder of glycosylation Ir
- congenital myasthenic syndrome 18
- autosomal recessive congenital ichthyosis 7
- congenital amegakaryocytic thrombocytopenia
- congenital myasthenic syndrome 5
- congenital diarrhea
- congenital disorder of glycosylation Im
- severe congenital encephalopathy due to MECP2 mutation
- congenital nongoitrous hypothyroidism 1
- congenital chylothorax
- congenital disorder of glycosylation Iy
- multiple congenital anomalies-hypotonia-seizures syndrome 2
- congenital dyserythropoietic anemia type IVa
- congenital disorder of glycosylation type IIb
- palmoplantar keratoderma and congenital alopecia 2
- lethal congenital glycogen storage disease of heart
- congenital merosin-deficient muscular dystrophy 1A
- congenital mirror movement disorder
- congenital disorder of glycosylation type IIk
- congenital fibrosis of the extraocular muscles
- congenital vertical talus
- congenital myasthenic syndrome 12
- congenital hypotrichosis with juvenile macular dystrophy
- congenital dyserythropoietic anemia type Ib
- congenital heart disease
- congenital disorder of glycosylation Iw
- X-linked congenital bilateral absence of vas deferens
- congenital disorder of glycosylation If
- lethal congenital contracture syndrome 2
- congenital myasthenic syndrome 2C
- congenital aphakia
- congenital afibrinogenemia
- congenital heart block
- congenital disorder of glycosylation type IIa
- congenital muscular dystrophy due to integrin alpha-7 deficiency
- congenital myasthenic syndrome 19
- congenital myopathy 4A
- large congenital melanocytic nevus
- multiple congenital anomalies-hypotonia-seizures syndrome 3
- multiple congenital anomalies-hypotonia-seizures syndrome
- congenital muscular dystrophy-dystroglycanopathy type A9
- congenital hypoplastic anemia
- congenital myasthenic syndrome 10
- congenital generalized lipodystrophy type 2
- congenital muscular dystrophy-dystroglycanopathy type A3
- congenital disorder of glycosylation type IIc
- autosomal dominant severe congenital neutropenia
- congenital dyserythropoietic anemia type I
- severe congenital neutropenia 4
- congenital stationary night blindness 1E
- congenital megabladder
- congenital generalized lipodystrophy
- Leber congenital amaurosis 9
- congenital muscular dystrophy-dystroglycanopathy type A10
- congenital stationary night blindness 1H
- congenital bile acid synthesis defect 6
- congenital mesoblastic nephroma
- congenital nongoitrous hypothyroidism 3
- congenital muscular dystrophy with cataracts and intellectual disability
- autosomal recessive congenital ichthyosis 11
- nonsyndromic congenital nail disorder 7
- lethal congenital contracture syndrome
- severe congenital neutropenia 8
- Leber congenital amaurosis 15
- congenital muscular dystrophy-dystroglycanopathy type A14
- nonsyndromic congenital nail disorder 2
- congenital muscular dystrophy-dystroglycanopathy type A11
- congenital syphilis
- congenital stationary night blindness
- congenital myasthenic syndrome 4A
- congenital sucrase-isomaltase deficiency
- congenital diarrhea 6
- congenital myasthenic syndrome 3A
- congenital myasthenic syndrome 4B
- nonsyndromic congenital nail disorder 4
- congenital myasthenic syndrome 17
- nonsyndromic congenital nail disorder
- congenital disorder of glycosylation Ig
- congenital disorder of glycosylation It
- congenital secretory sodium diarrhea 3
- Zika virus congenital syndrome
- Leber congenital amaurosis 4
- congenital heart defects, hamartomas of tongue, and polysyndactyly
- congenital muscular dystrophy-dystroglycanopathy type A
- congenital disorder of glycosylation type IIm
- congenital myasthenic syndrome 7
- non-congenital cyst of kidney
- congenital disorder of glycosylation Ie
- rapidly involuting congenital hemangioma
- Leber congenital amaurosis 6
- congenital dyserythropoietic anemia type II
- congenital secretory sodium diarrhea 8
- congenital ptosis
- congenital disorder of glycosylation type IId
- severe congenital neutropenia 6
- late congenital syphilis
- congenital disorder of glycosylation Ik
- congenital generalized lipodystrophy type 1
- linear skin defects with multiple congenital anomalies 1
- congenital muscular dystrophy-dystroglycanopathy type A2
- linear skin defects with multiple congenital anomalies 2
- congenital myasthenic syndrome 20
- congenital stationary night blindness 1G
- congenital stationary night blindness autosomal dominant 1
- severe congenital neutropenia
- congenital disorder of glycosylation Ic
- congenital bile acid synthesis defect
- congenital disorder of glycosylation type IIq
- X-linked congenital hemolytic anemia
- congenital myasthenic syndrome 11
- congenital stationary night blindness 1A
- nonsyndromic congenital nail disorder 3
- congenital granular cell tumor
- congenital central hypoventilation syndrome
- congenital fibrosarcoma
- congenital stationary night blindness 2A
- congenital hemolytic anemia
- congenital disorder of glycosylation Iu
- congenital disorder of glycosylation Ij
- congenital disorder of glycosylation type II
- congenital muscular dystrophy-dystroglycanopathy type A7
- severe congenital neutropenia 1
- congenital muscular dystrophy due to LMNA mutation
- congenital contractural arachnodactyly
- Leber congenital amaurosis 12
- X-linked congenital myopathy with fiber-type disproportion
- congenital leptin deficiency
- congenital disorder of glycosylation type IIp
- laryngomalacia
- autosomal recessive congenital ichthyosis 10
- congenital myasthenic syndrome 6
- congenital disorder of glycosylation Il
- congenital disorder of glycosylation type I
- autosomal recessive congenital ichthyosis 5
- nonsyndromic congenital nail disorder 8
- Leber congenital amaurosis 8
- autosomal dominant congenital deafness with onychodystrophy
- congenital myasthenic syndrome 9
- congenital stromal corneal dystrophy
- autosomal recessive congenital ichthyosis 8
- congenital nonspherocytic hemolytic anemia
- congenital nystagmus 7
- congenital hypothyroidism
- Leber congenital amaurosis 13
- congenital myasthenic syndrome 3C
- autosomal recessive congenital ichthyosis
- congenital disorder of glycosylation type IIn
- congenital nystagmus
- congenital structural myopathy
- autosomal recessive congenital ichthyosis 4B
- congenital myasthenic syndrome 2A
- blepharophimosis
- congenital nongoitrous hypothyroidism 4
- linear skin defects with multiple congenital anomalies 3
- congenital intrinsic factor deficiency
- congenital stationary night blindness autosomal dominant 2
- congenital nystagmus 1
- pancreatic hypoplasia-diabetes-congenital heart disease syndrome
- Ullrich congenital muscular dystrophy
- autosomal recessive congenital ichthyosis 4A
- congenital disorder of glycosylation Iaa
- congenital bile acid synthesis defect 1
- congenital disorder of glycosylation type IIi
- congenital disorder of glycosylation Ib
- congenital nongoitrous hypothyroidism 8
- autosomal recessive congenital ichthyosis 13
- epidermolysis bullosa with congenital localized absence of skin and deformity of nails
- palmoplantar keratoderma and congenital alopecia 1
- neonatal diabetes mellitus with congenital hypothyroidism
- congenital adrenal insufficiency
- lethal congenital contracture syndrome 1
- megaconial type congenital muscular dystrophy
- autosomal recessive congenital ichthyosis 3
- congenital disorder of glycosylation In
- congenital disorder of glycosylation Ix
- congenital toxoplasmosis
- Leber congenital amaurosis 16
- congenital muscular dystrophy-dystroglycanopathy type A8
- nonsyndromic congenital nail disorder 6
- Leber congenital amaurosis 1
- congenital epulis
- Leber congenital amaurosis 11
- congenital muscular dystrophy
- Leber congenital amaurosis 7
- autosomal recessive congenital ichthyosis 9
- congenital stationary night blindness autosomal dominant 3
- congenital muscular dystrophy 1B
- congenital disorder of glycosylation type IIj
- congenital diarrhea 5 with tufting enteropathy
- congenital dyserythropoietic anemia type IIIa
- congenital myasthenic syndrome 16
- congenital nystagmus 2
- congenital nongoitrous hypothyroidism 5
- congenital stationary night blindness 1F
- Leber congenital amaurosis 17
- spondyloepiphyseal dysplasia with congenital joint dislocations
- congenital diarrhea 7 with exudative enteropathy
- congenital nongoitrous hypothyroidism 9
- T-cell immunodeficiency, congenital alopecia, and nail dystrophy
- congenital dyserythropoietic anemia
- congenital stationary night blindness 1C
- nonsyndromic congenital nail disorder 5
- congenital myasthenic syndrome 1B
- multiple congenital anomalies-hypotonia-seizures syndrome 1
- lethal congenital contracture syndrome 3
- autosomal recessive congenital ichthyosis 14
- congenital nystagmus 3
- X-linked severe congenital neutropenia
- congenital disorder of glycosylation type IIf
- severe congenital neutropenia 7
- myotonia congenita
- congenital disorder of glycosylation type IIh
- congenital bile acid synthesis defect 5
- congenital lactase deficiency
- early congenital syphilis
- TORCH syndrome
- congenital secretory chloride diarrhea 1
- congenital nystagmus 5
- congenital myasthenic syndrome 15
- congenital generalized lipodystrophy type 4
- congenital adrenal hyperplasia
- congenital disorder of glycosylation Ip
- congenital disorder of glycosylation Id
- congenital myasthenic syndrome 4C
- congenital disorder of glycosylation
- congenital nongoitrous hypothyroidism 2
- congenital disorder of glycosylation type IIl
- congenital disorder of glycosylation type IIo
- severe congenital neutropenia 5
- congenital nystagmus 6
- arthrogryposis multiplex congenita
- congenital muscular dystrophy-dystroglycanopathy type A13
- congenital stationary night blindness 1B
- nonsyndromic congenital nail disorder 1
- congenital myasthenic syndrome
- congenital stationary night blindness 1D
- Leber congenital amaurosis 14
- congenital myasthenic syndrome 22
- congenital disorder of glycosylation type IIg
- congenital myasthenic syndrome 3B
- congenital bilateral absence of vas deferens
- Leber congenital amaurosis 3
- congenital disorder of glycosylation Ii
- congenital bile acid synthesis defect 4
- congenital disorder of glycosylation type IIe
- congenital myasthenic syndrome 8
- congenital generalized lipodystrophy type 3
- autosomal recessive congenital nystagmus
- congenital muscular dystrophy-dystroglycanopathy type A1
- lethal congenital contracture syndrome 4
- Leber congenital amaurosis 2
- congenital disorder of glycosylation Icc
- congenital bile acid synthesis defect 3
- Leber congenital amaurosis 5
- congenital disorder of glycosylation Ia
- cellular congenital mesoblastic nephroma