RGD DISEASE ONTOLOGY - ANNOTATIONS
RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term: hypohidrotic ectodermal dysplasia
Accession: DOID:14793
browse the term
Definition: An ectodermal dysplasia that is characterized by malformation of ectodermal (skin, hair, teeth and sweat glands) structures including hypotrichosis (sparseness of scalp and body hair), hypohidrosis (reduced ability to sweat), and hypodontia (congenital absence of teeth). (DO)
Synonyms: xref: GARD:76 ; NCI:C84562 ; ORDO:238468
For additional species annotation, visit the
Alliance of Genome Resources .
G
EDA
ectodysplasin A
ISO
ClinVar Annotator: match by term: Hypohidrotic X-linked ectodermal dysplasia
ClinVar
PMID:8696334 PMID:9507389 PMID:9536098 PMID:9630076 PMID:9683615 PMID:9736768 PMID:9856856 PMID:10951256 PMID:11279189 PMID:11295832 PMID:11309369 PMID:11378824 PMID:11416205 PMID:12930312 PMID:12949972 PMID:14656435 PMID:15461765 PMID:15663448 PMID:16199547 PMID:17066260 PMID:17576681 PMID:17970812 PMID:18076698 PMID:18231121 PMID:18384562 PMID:18386312 PMID:18386315 PMID:18427821 PMID:18451855 PMID:18510547 PMID:18545687 PMID:18657636 PMID:18666859 PMID:18821982 PMID:19278982 PMID:19533796 PMID:19592680 PMID:19623212 PMID:19921643 PMID:20236127 PMID:20374512 PMID:20486090 PMID:20979233 PMID:21357618 PMID:21457804 PMID:22032522 PMID:22382802 PMID:22428923 PMID:22633615 PMID:22875504 PMID:23293949 PMID:23553579 PMID:23744313 PMID:23926003 PMID:23989902 PMID:23991204 PMID:24033266 PMID:24279917 PMID:24312213 PMID:24330993 PMID:24487376 PMID:24648697 PMID:24689965 PMID:24724966 PMID:25333067 PMID:25626993 PMID:25741868 PMID:26273176 PMID:26345974 PMID:26634545 PMID:26753551 PMID:27054699 PMID:27144394 PMID:27305980 PMID:27538153 PMID:27657131 PMID:28045201 PMID:28492532 PMID:29444360 PMID:30117778 PMID:31306530 PMID:31796081 PMID:31924237 More...
NCBI chr X:54,078,694...54,515,535
Ensembl chr X:54,078,966...54,515,535
G
EDAR
ectodysplasin A receptor
ISO
ClinVar Annotator: match by term: Hypohidrotic ectodermal dysplasia
ClinVar
PMID:18065779 PMID:18561327 PMID:18704500 PMID:24033266 PMID:25741868 PMID:28492532 PMID:28808699 More...
NCBI chr10:34,873,311...34,943,140
Ensembl chr10:34,848,526...34,940,784
G
EDARADD
EDAR associated death domain
ISO
ClinVar Annotator: match by term: Hypohidrotic ectodermal dysplasia
ClinVar
PMID:20222921 PMID:20979233 PMID:21448560 PMID:21626677 PMID:25741868 PMID:28492532 More...
NCBI chr 4:3,608,545...3,659,357
Ensembl chr 4:3,610,079...3,669,789
G
RANBP2
RAN binding protein 2
ISO
ClinVar Annotator: match by term: Hypohidrotic ectodermal dysplasia
ClinVar
PMID:18065779 PMID:18561327 PMID:18704500 PMID:24033266 PMID:25741868 PMID:28492532 PMID:28808699 More...
NCBI chr10:35,088,175...35,181,248
Ensembl chr10:35,088,872...35,181,129
G
TRAF6
TNF receptor associated factor 6
ISO
OMIM:129490 | OMIM:224900 | OMIM:300291 | OMIM:305100
MouseDO
NCBI chr18:31,674,242...31,689,160
Ensembl chr18:31,675,391...31,688,641
G
WNT10A
Wnt family member 10A
ISO
ClinVar Annotator: match by term: Hypohidrotic ectodermal dysplasia
ClinVar
PMID:19559398 PMID:20979233 PMID:21279306 PMID:21484994 PMID:22581971 PMID:23401279 PMID:24033266 PMID:24449199 PMID:24700731 PMID:25629078 PMID:25713620 PMID:25741868 PMID:26964878 PMID:27881089 PMID:28105635 PMID:28492532 PMID:28813618 PMID:28976000 PMID:29364747 PMID:30426266 PMID:30974434 PMID:35537890 More...
NCBI chr37:25,463,064...25,475,407
Ensembl chr37:25,462,748...25,474,764
G
EDA
ectodysplasin A
ISO
ClinVar Annotator: match by term: Hypohidrotic X-linked ectodermal dysplasia
OMIM ClinVar
PMID:8696334 PMID:9507389 PMID:9536098 PMID:9630076 PMID:9683615 PMID:9736768 PMID:9856856 PMID:10469321 PMID:10951256 PMID:11279189 PMID:11295832 PMID:11309369 PMID:11378824 PMID:11416205 PMID:12930312 PMID:12947561 PMID:12949972 PMID:14656435 PMID:15461765 PMID:15663448 PMID:16199547 PMID:17066260 PMID:17576681 PMID:17970812 PMID:18076698 PMID:18231121 PMID:18384562 PMID:18386312 PMID:18386315 PMID:18427821 PMID:18451855 PMID:18510547 PMID:18545687 PMID:18657636 PMID:18666859 PMID:18688569 PMID:18821982 PMID:19278982 PMID:19438931 PMID:19504606 PMID:19533796 PMID:19592680 PMID:19623212 PMID:19921643 PMID:19960895 PMID:20077893 PMID:20236127 PMID:20374512 PMID:20486090 PMID:20979233 PMID:21357618 PMID:21457804 PMID:22032522 PMID:22382802 PMID:22428923 PMID:22633615 PMID:22875504 PMID:23293949 PMID:23553579 PMID:23687000 PMID:23744313 PMID:23926003 PMID:23989902 PMID:23991204 PMID:24033266 PMID:24279917 PMID:24312213 PMID:24330993 PMID:24487376 PMID:24631698 PMID:24648697 PMID:24689965 PMID:24715423 PMID:24724966 PMID:25333067 PMID:25626993 PMID:25640679 PMID:25741868 PMID:25741905 PMID:25846883 PMID:26273176 PMID:26345974 PMID:26411740 PMID:26634545 PMID:26753551 PMID:27054699 PMID:27144394 PMID:27264909 PMID:27305980 PMID:27538153 PMID:27657131 PMID:28045201 PMID:28492532 PMID:29444360 PMID:29676859 PMID:30088137 PMID:30117778 PMID:31129666 PMID:31306530 PMID:31489414 PMID:31652981 PMID:31796081 PMID:31852928 PMID:31924237 PMID:33205897 PMID:33502802 PMID:33943035 PMID:34573371 PMID:34863015 PMID:34906502 PMID:35023123 PMID:36071541 PMID:36294409 PMID:202361270 More...
NCBI chr X:54,078,694...54,515,535
Ensembl chr X:54,078,966...54,515,535
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MVK
mevalonate kinase
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 1, anhidrotic
ClinVar
PMID:25741868
NCBI chr26:17,497,516...17,519,015
Ensembl chr26:17,497,513...17,519,385
G
CCDC138
coiled-coil domain containing 138
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant
ClinVar
PMID:10431241 PMID:10431242 PMID:18854857 PMID:20979233 PMID:28492532 PMID:28981473 More...
NCBI chr10:34,976,341...35,086,080
Ensembl chr10:34,976,670...35,086,297
G
EDAR
ectodysplasin A receptor
ISO
ClinVar Annotator: match by term: Autosomal dominant hypohidrotic ectodermal dysplasia | ClinVar Annotator: match by term: Ectodermal Dysplasia 3, Anhidrotic | ClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant | ClinVar Annotator: match by term: Ectodermal dysplasia 10a, hypohidrotic/hair/tooth type, autosomal dominant
OMIM ClinVar
PMID:9536098 PMID:10431241 PMID:10431242 PMID:11035039 PMID:11279189 PMID:15013427 PMID:16029325 PMID:16199547 PMID:16435307 PMID:17125505 PMID:17576681 PMID:18065779 PMID:18231121 PMID:18561327 PMID:18704500 PMID:18854857 PMID:19438931 PMID:20236127 PMID:20979233 PMID:21771270 PMID:21876339 PMID:22032522 PMID:23401279 PMID:23991204 PMID:24033266 PMID:24641098 PMID:24884697 PMID:25741868 PMID:26336973 PMID:27305980 PMID:27657131 PMID:28265457 PMID:28492532 PMID:28981473 PMID:32274043 PMID:32325225 PMID:33205897 More...
NCBI chr10:34,873,311...34,943,140
Ensembl chr10:34,848,526...34,940,784
G
EDARADD
EDAR associated death domain
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant
ClinVar
PMID:9245989 PMID:11780064 PMID:17354266 PMID:20222921
NCBI chr 4:3,608,545...3,659,357
Ensembl chr 4:3,610,079...3,669,789
G
GCC2
GRIP and coiled-coil domain containing 2
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant
ClinVar
PMID:10431241 PMID:10431242 PMID:18854857 PMID:20979233 PMID:28492532 PMID:28981473 More...
NCBI chr10:35,379,055...35,431,500
Ensembl chr10:35,379,030...35,431,457
G
LIMS1
LIM zinc finger domain containing 1
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant
ClinVar
PMID:10431241 PMID:10431242 PMID:18854857 PMID:20979233 PMID:28492532 PMID:28981473 More...
NCBI chr10:35,192,582...35,339,100
G
RANBP2
RAN binding protein 2
ISO
ClinVar Annotator: match by term: Autosomal dominant hypohidrotic ectodermal dysplasia | ClinVar Annotator: match by term: Ectodermal Dysplasia 3, Anhidrotic | ClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant | ClinVar Annotator: match by term: Ectodermal dysplasia 10a, hypohidrotic/hair/tooth type, autosomal dominant
ClinVar
PMID:9536098 PMID:10431241 PMID:10431242 PMID:11035039 PMID:11279189 PMID:15013427 PMID:16029325 PMID:16199547 PMID:16435307 PMID:17125505 PMID:17576681 PMID:18065779 PMID:18231121 PMID:18561327 PMID:18704500 PMID:18854857 PMID:19438931 PMID:20236127 PMID:20979233 PMID:21771270 PMID:21876339 PMID:22032522 PMID:23401279 PMID:23991204 PMID:24033266 PMID:24641098 PMID:24884697 PMID:25741868 PMID:26336973 PMID:27305980 PMID:27657131 PMID:28265457 PMID:28492532 PMID:28981473 PMID:32274043 PMID:32325225 PMID:33205897 More...
NCBI chr10:35,088,175...35,181,248
Ensembl chr10:35,088,872...35,181,129
G
SLC5A7
solute carrier family 5 member 7
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant
ClinVar
PMID:10431241 PMID:10431242 PMID:18854857 PMID:20979233 PMID:28492532 PMID:28981473 More...
NCBI chr10:35,879,880...35,908,203
Ensembl chr10:35,883,245...35,908,569
G
SULT1C2
sulfotransferase family 1C member 2
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant
ClinVar
PMID:10431241 PMID:10431242 PMID:18854857 PMID:20979233 PMID:28492532 PMID:28981473 More...
NCBI chr10:35,561,023...35,589,999
Ensembl chr10:35,563,044...35,578,434
G
SULT1C3
sulfotransferase family 1C member 3
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant
ClinVar
PMID:10431241 PMID:10431242 PMID:18854857 PMID:20979233 PMID:28492532 PMID:28981473 More...
NCBI chr10:35,610,282...35,644,315
Ensembl chr10:35,610,989...35,644,557
G
SULT1C4
sulfotransferase family 1C member 4
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant
ClinVar
PMID:10431241 PMID:10431242 PMID:18854857 PMID:20979233 PMID:28492532 PMID:28981473 More...
NCBI chr10:35,494,614...35,504,162
Ensembl chr10:35,495,727...35,504,125
G
CCDC138
coiled-coil domain containing 138
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive
ClinVar
PMID:28492532
NCBI chr10:34,976,341...35,086,080
Ensembl chr10:34,976,670...35,086,297
G
EDAR
ectodysplasin A receptor
ISO
ClinVar Annotator: match by term: Autosomal recessive hypohidrotic ectodermal dysplasia | ClinVar Annotator: match by term: Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive | ClinVar Annotator: match by term: Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive
OMIM ClinVar
PMID:10431241 PMID:11279189 PMID:15373768 PMID:16435307 PMID:18065779 PMID:18231121 PMID:18561327 PMID:18704500 PMID:18816645 PMID:20236127 PMID:20979233 PMID:22032522 PMID:24033266 PMID:25741868 PMID:28492532 More...
NCBI chr10:34,873,311...34,943,140
Ensembl chr10:34,848,526...34,940,784
G
EDARADD
EDAR associated death domain
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive
ClinVar
NCBI chr 4:3,608,545...3,659,357
Ensembl chr 4:3,610,079...3,669,789
G
RANBP2
RAN binding protein 2
ISO
ClinVar Annotator: match by term: Autosomal recessive hypohidrotic ectodermal dysplasia | ClinVar Annotator: match by term: Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive | ClinVar Annotator: match by term: Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive
ClinVar
PMID:10431241 PMID:11279189 PMID:15373768 PMID:16435307 PMID:18065779 PMID:18231121 PMID:18561327 PMID:18704500 PMID:18816645 PMID:20236127 PMID:20979233 PMID:22032522 PMID:24033266 PMID:25741868 PMID:28492532 More...
NCBI chr10:35,088,175...35,181,248
Ensembl chr10:35,088,872...35,181,129
G
EDARADD
EDAR associated death domain
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant
OMIM ClinVar
PMID:11780064 PMID:17354266 PMID:20222921 PMID:20979233 PMID:21626677 PMID:25640679 PMID:25741868 PMID:26440664 PMID:28492532 PMID:33502802 PMID:34219261 PMID:34573371 More...
NCBI chr 4:3,608,545...3,659,357
Ensembl chr 4:3,610,079...3,669,789
G
EDAR
ectodysplasin A receptor
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive
ClinVar
PMID:10431241 PMID:11035039 PMID:15013427 PMID:16435307 PMID:18231121 PMID:20979233 PMID:23401279 PMID:25741868 PMID:27657131 PMID:28492532 More...
NCBI chr10:34,873,311...34,943,140
Ensembl chr10:34,848,526...34,940,784
G
EDARADD
EDAR associated death domain
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive | ClinVar Annotator: match by term: Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive
OMIM ClinVar
PMID:9245989 PMID:11212737 PMID:11780064 PMID:17354266 PMID:25741868 PMID:26440664 PMID:26991760 PMID:28492532 PMID:34219261 More...
NCBI chr 4:3,608,545...3,659,357
Ensembl chr 4:3,610,079...3,669,789
G
RANBP2
RAN binding protein 2
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive
ClinVar
PMID:10431241 PMID:11035039 PMID:15013427 PMID:16435307 PMID:18231121 PMID:20979233 PMID:23401279 PMID:25741868 PMID:27657131 PMID:28492532 More...
NCBI chr10:35,088,175...35,181,248
Ensembl chr10:35,088,872...35,181,129
G
KDF1
keratinocyte differentiation factor 1
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type
OMIM ClinVar
PMID:25741868 PMID:27838789 PMID:28492532
NCBI chr 2:73,198,278...73,206,691
Ensembl chr 2:73,197,580...73,207,153
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CST6
cystatin E/M
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia 15, hypohidrotic/hair type
OMIM ClinVar
PMID:25741868 PMID:25741909 PMID:30425301
NCBI chr18:51,263,161...51,264,816
Ensembl chr18:51,263,178...51,264,780
G
G6PD
glucose-6-phosphate dehydrogenase
ISO
ClinVar Annotator: match by term: ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNE DEFICIENCY
ClinVar
PMID:25741868
NCBI chr X:122,217,317...122,231,862
Ensembl chr X:122,205,683...122,231,678
G
IKBKG
inhibitor of nuclear factor kappa B kinase regulatory subunit gamma
ISO
ClinVar Annotator: match by term: ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNE DEFICIENCY
ClinVar
PMID:25741868
NCBI chr X:122,232,052...122,253,499
Ensembl chr X:122,235,878...122,250,562
G
G6PD
glucose-6-phosphate dehydrogenase
ISO
ClinVar Annotator: match by term: Hyper-IgM immunodeficiency, X-linked, with hypohidrotic ectodermal dysplasia
ClinVar
PMID:25741868
NCBI chr X:122,217,317...122,231,862
Ensembl chr X:122,205,683...122,231,678
G
IKBKG
inhibitor of nuclear factor kappa B kinase regulatory subunit gamma
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia and immunodeficiency 1 | ClinVar Annotator: match by term: Hyper-IgM immunodeficiency, X-linked, with hypohidrotic ectodermal dysplasia
OMIM ClinVar
PMID:11242109 PMID:11590134 PMID:15229184 PMID:15833888 PMID:16532398 PMID:16818673 PMID:16950813 PMID:17072331 PMID:17910706 PMID:18222329 PMID:18851874 PMID:19903677 PMID:21622647 PMID:24682681 PMID:25741868 PMID:26117626 PMID:28993958 PMID:29077208 PMID:30422821 PMID:31965418 PMID:33224153 More...
NCBI chr X:122,232,052...122,253,499
Ensembl chr X:122,235,878...122,250,562
G
BAZ1A
bromodomain adjacent to zinc finger domain 1A
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia and immunodeficiency 2
ClinVar
PMID:28492532
NCBI chr 8:13,604,694...13,694,508
Ensembl chr 8:13,605,182...13,693,847
G
CFL2
cofilin 2
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia and immunodeficiency 2
ClinVar
PMID:28492532
NCBI chr 8:13,578,152...13,582,408
Ensembl chr 8:13,580,360...13,582,442
G
FAM177A1
family with sequence similarity 177 member A1
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia and immunodeficiency 2
ClinVar
PMID:28492532
NCBI chr 8:13,844,565...13,862,619
Ensembl chr 8:13,844,685...13,860,889
G
NFKBIA
NFKB inhibitor alpha
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia and immunodeficiency 2 | ClinVar Annotator: match by term: Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant
OMIM ClinVar
PMID:9536098 PMID:14523047 PMID:15337789 PMID:17576681 PMID:17931563 PMID:18412279 PMID:23708964 PMID:23864385 PMID:23870671 PMID:24033266 PMID:25601653 PMID:25741868 PMID:26888281 PMID:28417298 PMID:28492532 PMID:28629746 PMID:29948576 PMID:32581362 PMID:32750042 More...
NCBI chr 8:14,100,203...14,103,453
Ensembl chr 8:14,100,671...14,103,433
G
PPP2R3C
protein phosphatase 2 regulatory subunit B''gamma
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia and immunodeficiency 2
ClinVar
PMID:28492532
NCBI chr 8:13,863,017...13,885,245
Ensembl chr 8:13,863,380...13,885,130
G
PRORP
protein only RNase P catalytic subunit
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia and immunodeficiency 2
ClinVar
PMID:28492532
NCBI chr 8:13,885,734...14,007,224
G
PSMA6
proteasome 20S subunit alpha 6
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia and immunodeficiency 2
ClinVar
PMID:28492532
NCBI chr 8:14,010,899...14,038,141
Ensembl chr 8:14,010,939...14,038,134
G
SRP54
signal recognition particle 54
ISO
ClinVar Annotator: match by term: Ectodermal dysplasia and immunodeficiency 2
ClinVar
PMID:28492532
NCBI chr 8:13,800,275...13,837,799
Ensembl chr 8:13,677,760...13,837,722
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