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Ontology Browser
Term:
multiple congenital anomalies-hypotonia-seizures syndrome 2 (DOID:0080139)
Annotations: Rat: (13) Mouse: (13) Human: (14) Chinchilla: (13) Bonobo: (13) Dog: (13) Squirrel: (13) Pig: (13) Naked Mole-rat: (13) Green Monkey: (13)
Parent Terms Term With Siblings Child Terms
adrenoleukodystrophy +   
Aland Island eye disease  
Allan-Herndon-Dudley syndrome  
AUTOINFLAMMATORY SYNDROME, FAMILIAL, X-LINKED, BEHCET-LIKE 2  
Barth syndrome +   
blue cone monochromacy  
Borjeson-Forssman-Lehmann syndrome  
Brunner syndrome  
CD40 ligand deficiency +   
Charcot-Marie-Tooth disease X-linked recessive 2 
Charcot-Marie-Tooth disease X-linked recessive 3 
Charcot-Marie-Tooth disease X-linked recessive 4  
Charcot-Marie-Tooth disease X-linked recessive 5  
CK syndrome  
combined oxidative phosphorylation deficiency 6  
congenital disorder of glycosylation Icc  
congenital disorder of glycosylation Iy  
congenital disorder of glycosylation type IIm  
congenital disorder of glycosylation type IIr  
congenital nongoitrous hypothyroidism 9  
congenital nonspherocytic hemolytic anemia 9  
congenital stationary night blindness 1A  
congenital stationary night blindness 2A  
Dent disease +   
developmental and epileptic encephalopathy 1  
developmental and epileptic encephalopathy 100  
developmental and epileptic encephalopathy 101  
developmental and epileptic encephalopathy 102  
developmental and epileptic encephalopathy 103  
developmental and epileptic encephalopathy 104  
developmental and epileptic encephalopathy 105  
developmental and epileptic encephalopathy 106  
developmental and epileptic encephalopathy 107  
developmental and epileptic encephalopathy 108  
developmental and epileptic encephalopathy 109  
developmental and epileptic encephalopathy 11  
developmental and epileptic encephalopathy 110  
Developmental and Epileptic Encephalopathy 111  
Developmental and Epileptic Encephalopathy 112  
Developmental and Epileptic Encephalopathy 113  
Developmental and Epileptic Encephalopathy 114  
Developmental and Epileptic Encephalopathy 115  
developmental and epileptic encephalopathy 116  
developmental and epileptic encephalopathy 12  
developmental and epileptic encephalopathy 13  
developmental and epileptic encephalopathy 14  
developmental and epileptic encephalopathy 15  
developmental and epileptic encephalopathy 16  
developmental and epileptic encephalopathy 17  
developmental and epileptic encephalopathy 18  
developmental and epileptic encephalopathy 19  
developmental and epileptic encephalopathy 2  
developmental and epileptic encephalopathy 21  
developmental and epileptic encephalopathy 23  
developmental and epileptic encephalopathy 24  
developmental and epileptic encephalopathy 25  
developmental and epileptic encephalopathy 26  
developmental and epileptic encephalopathy 27  
developmental and epileptic encephalopathy 28  
developmental and epileptic encephalopathy 29  
developmental and epileptic encephalopathy 3  
developmental and epileptic encephalopathy 30  
developmental and epileptic encephalopathy 31A  
developmental and epileptic encephalopathy 31B  
developmental and epileptic encephalopathy 32  
developmental and epileptic encephalopathy 33  
developmental and epileptic encephalopathy 34  
developmental and epileptic encephalopathy 35  
developmental and epileptic encephalopathy 36  
developmental and epileptic encephalopathy 37  
developmental and epileptic encephalopathy 38  
developmental and epileptic encephalopathy 39  
developmental and epileptic encephalopathy 4  
developmental and epileptic encephalopathy 40  
developmental and epileptic encephalopathy 41  
developmental and epileptic encephalopathy 42  
developmental and epileptic encephalopathy 43  
developmental and epileptic encephalopathy 44  
developmental and epileptic encephalopathy 45  
developmental and epileptic encephalopathy 46  
developmental and epileptic encephalopathy 47  
developmental and epileptic encephalopathy 48  
developmental and epileptic encephalopathy 49  
developmental and epileptic encephalopathy 5  
developmental and epileptic encephalopathy 50  
developmental and epileptic encephalopathy 51  
developmental and epileptic encephalopathy 52  
developmental and epileptic encephalopathy 53  
developmental and epileptic encephalopathy 54  
developmental and epileptic encephalopathy 55  
developmental and epileptic encephalopathy 56  
developmental and epileptic encephalopathy 57  
developmental and epileptic encephalopathy 58  
developmental and epileptic encephalopathy 59  
developmental and epileptic encephalopathy 60  
developmental and epileptic encephalopathy 61  
developmental and epileptic encephalopathy 62  
developmental and epileptic encephalopathy 63  
developmental and epileptic encephalopathy 64  
developmental and epileptic encephalopathy 65  
developmental and epileptic encephalopathy 66  
developmental and epileptic encephalopathy 67  
developmental and epileptic encephalopathy 68  
developmental and epileptic encephalopathy 69  
developmental and epileptic encephalopathy 6B  
developmental and epileptic encephalopathy 7  
developmental and epileptic encephalopathy 70  
developmental and epileptic encephalopathy 71  
developmental and epileptic encephalopathy 72  
developmental and epileptic encephalopathy 73  
developmental and epileptic encephalopathy 74  
developmental and epileptic encephalopathy 75  
developmental and epileptic encephalopathy 76  
developmental and epileptic encephalopathy 78  
developmental and epileptic encephalopathy 79  
developmental and epileptic encephalopathy 8  
developmental and epileptic encephalopathy 80  
developmental and epileptic encephalopathy 81  
developmental and epileptic encephalopathy 82  
developmental and epileptic encephalopathy 83  
developmental and epileptic encephalopathy 84  
developmental and epileptic encephalopathy 85  
developmental and epileptic encephalopathy 86  
developmental and epileptic encephalopathy 87  
developmental and epileptic encephalopathy 88  
developmental and epileptic encephalopathy 89  
developmental and epileptic encephalopathy 9  
developmental and epileptic encephalopathy 90  
developmental and epileptic encephalopathy 91  
developmental and epileptic encephalopathy 92  
developmental and epileptic encephalopathy 93  
developmental and epileptic encephalopathy 94  
developmental and epileptic encephalopathy 95  
developmental and epileptic encephalopathy 96  
developmental and epileptic encephalopathy 97  
developmental and epileptic encephalopathy 98  
developmental and epileptic encephalopathy 99  
Diamond-Blackfan anemia 14 with mandibulofacial dysostosis  
Dravet syndrome  
Duchenne muscular dystrophy +   
ectodermal dysplasia 1 +   
factor VIII deficiency +   
Fanconi anemia complementation group B  
FG syndrome +   
frontometaphyseal dysplasia 1  
Galloway-Mowat syndrome 2  
glycogen storage disease IXA  
glycogen storage disease IXD  
glycogen storage disease VIII  
hemophilia B  
hereditary sensory neuropathy X-linked 
hereditary spastic paraplegia 16 
hereditary spastic paraplegia 2  
hereditary spastic paraplegia 34 
Holoprosencephaly 13, X-linked  
HRPT-related hyperuricemia  
hypogonadotropic hypogonadism 1 with or without anosmia  
ichthyosis follicularis-alopecia-photophobia syndrome 1  
IGSF1 deficiency syndrome  
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome  
immunodeficiency 102  
immunodeficiency 118  
immunodeficiency 33  
immunodeficiency 34  
immunodeficiency 47  
immunodeficiency 50  
immunodeficiency 98  
isolated growth hormone deficiency type III  
Joubert syndrome 10  
Keipert syndrome  
Kennedy's disease  
Lesch-Nyhan syndrome +   
MASA syndrome  
megalocornea +   
MEHMO syndrome  
MEND syndrome  
methylmalonic acidemia and homocysteinemia cblX type  
microcephaly, seizures, and developmental delay  
midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis  
Mullegama-Klein-Martinez syndrome  
multiple congenital anomalies-hypotonia-seizures syndrome 1  
multiple congenital anomalies-hypotonia-seizures syndrome 2  
A multiple congenital anomalies-hypotonia-seizures syndrome that is characterized by X-linked recessive inheritance of dysmorphic features, neonatal hypotonia, myoclonic seizures and variable abnormalities involving the central nervous, cardiac, and urinary systems that has_material_basis_in mutation in the PIGA gene on chromosome Xp22. (DO)
multiple congenital anomalies-hypotonia-seizures syndrome 3  
multiple congenital anomalies-hypotonia-seizures syndrome 4  
nephrogenic syndrome of inappropriate antidiuresis  
non-syndromic X-linked intellectual disability 100  
non-syndromic X-linked intellectual disability 101  
non-syndromic X-linked intellectual disability 103  
non-syndromic X-linked intellectual disability 104  
non-syndromic X-linked intellectual disability 105  
non-syndromic X-linked intellectual disability 21  
non-syndromic X-linked intellectual disability 30  
non-syndromic X-linked intellectual disability 46  
non-syndromic X-linked intellectual disability 53 
non-syndromic X-linked intellectual disability 58  
non-syndromic X-linked intellectual disability 72  
non-syndromic X-linked intellectual disability 73 
non-syndromic X-linked intellectual disability 77 
non-syndromic X-linked intellectual disability 81 
non-syndromic X-linked intellectual disability 82 
non-syndromic X-linked intellectual disability 84 
non-syndromic X-linked intellectual disability 9  
non-syndromic X-linked intellectual disability 90  
non-syndromic X-linked intellectual disability 92 
non-syndromic X-linked intellectual disability 93  
non-syndromic X-linked intellectual disability 96  
non-syndromic X-linked intellectual disability 99  
non-syndromic X-linked intellectual disability ARX-related  
Norrie disease  
nuclear type mitochondrial complex I deficiency 12  
nuclear type mitochondrial complex I deficiency 30  
occipital horn syndrome  
oculocerebrorenal syndrome +   
Opitz GBBB syndrome  
orofaciodigital syndrome VIII 
osteogenesis imperfecta type 19  
Paganini-Miozzo syndrome  
partial androgen insensitivity syndrome  
Partington syndrome  
Pelizaeus-Merzbacher disease +   
phosphoglycerate kinase 1 deficiency  
phosphoribosylpyrophosphate synthetase superactivity  
Prieto syndrome  
primary ovarian insufficiency 2B  
Renpenning syndrome  
retinitis pigmentosa 23  
Ritscher-Schinzel syndrome 2  
severe congenital encephalopathy due to MECP2 mutation  
Shukla-Vernon syndrome  
sideroblastic anemia 1  
Simpson-Golabi-Behmel syndrome type 1  
Simpson-Golabi-Behmel syndrome type 2  
spastic paraplegia with deafness 
syndactyly type 8  
syndromic X-linked intellectual disability 17 
syndromic X-linked intellectual disability 35  
syndromic X-linked intellectual disability 5  
syndromic X-linked intellectual disability Claes-Jensen type  
syndromic X-linked intellectual disability Siderius type  
syndromic X-linked intellectual disability Snyder type  
syndromic X-linked intellectual disability Turner type  
syndromic X-linked intellectual disorder Lujan-Fryns-type  
Van Esch-O'Driscoll syndrome  
visceral heterotaxy 1  
Waisman syndrome  
Wieacker-Wolff syndrome  
Wilson-Turner syndrome  
Wiskott-Aldrich syndrome +   
X-linked Aarskog syndrome  
X-linked adrenal hypoplasia congenita  
X-linked agammaglobulinemia +   
X-linked atrophic macular degeneration  
X-linked chondrodysplasia punctata 1  
X-linked chronic granulomatous disease  
X-linked chronic idiopathic intestinal pseudo-obstruction  
X-linked cone-rod dystrophy 3  
X-linked congenital hemolytic anemia  
X-linked deafness 5  
X-linked distal spinal muscular atrophy 3  
X-linked dyserythropoietic anemia  
X-linked dyskeratosis congenita +   
X-linked dystonia-parkinsonism  
X-linked Emery-Dreifuss muscular dystrophy 1  
X-linked Emery-Dreifuss muscular dystrophy 6  
X-linked hyper IgM syndrome  
X-linked ichthyosis +   
X-Linked immunodeficiency 74  
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia  
X-linked intellectual developmental disorder 108  
X-linked intellectual developmental disorder 109  
X-linked intellectual disability-short stature-overweight syndrome  
X-linked juvenile retinoschisis 1  
X-linked keratosis follicularis spinulosa decalvans  
X-linked lymphoproliferative syndrome 1  
X-linked lymphoproliferative syndrome 2  
X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques  
X-linked myopathy with excessive autophagy  
X-linked nephrogenic diabetes insipidus  
X-linked nephrolithiasis type I  
X-linked parkinsonism-spasticity syndrome  
X-linked properdin deficiency  
X-linked recessive hypophosphatemic rickets  
X-linked severe combined immunodeficiency  
X-linked severe congenital neutropenia  
X-linked sideroblastic anemia with ataxia  
X-linked spermatogenic failure 2  
X-linked spermatogenic failure 3  
X-linked spermatogenic failure 7  
X-linked spinal muscular atrophy 2  
X-linked spinocerebellar ataxia 1  
X-linked spinocerebellar ataxia 5 
X-linked spondyloepimetaphyseal dysplasia +   
X-linked spondyloepiphyseal dysplasia tarda  
X-linked thrombocytopenia with beta-thalassemia  
X-linked VACTERL association  

Synonyms
Exact Synonyms: DEE20 ;   EIEE20 ;   GPIBD4 ;   MCAHS2 ;   developmental and epileptic encephalopathy 20 ;   early infantile epileptic encephalopathy 20 ;   glycosylphosphatidylinositol biosynthesis defect 4
Primary IDs: MIM:300868
Alternate IDs: DOID:0080466
Xrefs: GARD:12777 ;   ORDO:300496
Definition Sources: PMID:10441586 "DO" "DO", PMID:22305531 "DO" "DO"

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