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Pediatric Disease Annotations & Medicines



   biotinidase deficiency
  

Disease ID 10
Disease biotinidase deficiency
Definition
A genetic disorder caused by mutations in the BTD gene. It is characterized by reduced or absent activity of the enzyme biotinidase which is responsible for the recycling of the vitamin biotin. Signs and symptoms appear in childhood and include seizures, hypotonia and developmental delays. If left untreated, it leads to vision and hearing loss, infections, alopecia and ataxia.
Synonym
biotinidase defic
biotinidase deficiencies
biotinidase deficiency (disorder)
biotinidase deficiency [disease/finding]
btd deficiencies
btd deficiency
carboxylase defic multiple late onset
carboxylase deficiency, multiple, late-onset
defic biotinidase
defic multiple carboxylase late onset
deficiencies, biotinidase
deficiencies, btd
deficiency of biotinidase
deficiency of biotinidase (disorder)
deficiency, biotinidase
deficiency, btd
deficiency, multiple carboxylase, late-onset
late onset biotin responsive multiple carboxylase deficiency
late onset multiple carboxylase deficiency
late-onset biotin-responsive multiple carboxylase deficiency
late-onset multiple carboxylase deficiency
multiple carboxylase defic late onset
multiple carboxylase deficiency - late onset
multiple carboxylase deficiency, late onset
multiple carboxylase deficiency, late-onset
Orphanet
OMIM
DOID
ICD10
UMLS
C0220754
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:5)
C0442874  |  neuropathy  |  1
C0014544  |  epilepsy  |  1
C0027813  |  neuritis  |  1
C0029124  |  optic atrophy  |  1
C0029132  |  optic neuropathy  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
BTD  |  686  |  CLINVAR;CTD_human;GHR;ORPHANET;UNIPROT
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:1)
686  |  BTD  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:30)
2639  |  GCDH  |  DISEASES
33  |  ACADL  |  DISEASES
7166  |  TPH1  |  DISEASES
3431  |  SP110  |  DISEASES
26525  |  IL36RN  |  DISEASES
2184  |  FAH  |  DISEASES
23531  |  MMD  |  DISEASES
28960  |  DCPS  |  DISEASES
1356  |  CP  |  DISEASES
4594  |  MUT  |  DISEASES
760  |  CA2  |  DISEASES
7200  |  TRH  |  DISEASES
6323  |  SCN1A  |  DISEASES
686  |  BTD  |  DISEASES
8884  |  SLC5A6  |  DISEASES
219541  |  MED19  |  DISEASES
3141  |  HLCS  |  DISEASES
64087  |  MCCC2  |  DISEASES
875  |  CBS  |  DISEASES
538  |  ATP7A  |  DISEASES
1056  |  CEL  |  DISEASES
2170  |  FABP3  |  DISEASES
3980  |  LIG3  |  DISEASES
5091  |  PC  |  DISEASES
95  |  ACY1  |  DISEASES
3033  |  HADH  |  DISEASES
7311  |  UBA52  |  DISEASES
8890  |  EIF2B4  |  DISEASES
3712  |  IVD  |  DISEASES
5096  |  PCCB  |  DISEASES
Locus
Symbol | Locus(Total Locus:1)
BTD  |  3p25.1
Disease ID 10
Disease biotinidase deficiency
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:23)
HP:0001317  |  Abnormality of the cerebellum
HP:0001324  |  Muscle weakness
HP:0001263  |  Global developmental delay
HP:0002104  |  Apnea
HP:0011127  |  Perioral eczema
HP:0001596  |  Alopecia
HP:0001251  |  Ataxia
HP:0000545  |  Myopia
HP:0001254  |  Lethargy
HP:0001510  |  Growth delay
HP:0005979  |  Metabolic ketoacidosis
HP:0001276  |  Hypertonia
HP:0001096  |  Keratoconjunctivitis
HP:0000365  |  Hearing impairment
HP:0001252  |  Muscular hypotonia
HP:0001259  |  Coma
HP:0001123  |  Visual field defect
HP:0002123  |  Generalized myoclonic seizures
HP:0007730  |  Iris hypopigmentation
HP:0006511  |  Laryngeal stridor
HP:0000648  |  Optic atrophy
HP:0002883  |  Hyperventilation
HP:0002841  |  Recurrent fungal infections
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:8)
HP:0001298  |  Encephalopathy  |  2
HP:0001250  |  Seizures  |  2
HP:0002273  |  Tetraparesis  |  1
HP:0001285  |  Spastic tetraparesis  |  1
HP:0200134  |  Epileptic encephalopathy  |  1
HP:0001138  |  Damaged optic nerve  |  1
HP:0000648  |  Optic-nerve degeneration  |  1
HP:0040078  |  Axonal degeneration  |  1
Disease ID 10
Disease biotinidase deficiency
Manually Symptom
UMLS  | Name(Total Manually Symptoms:8)
C2029884  |  hearing loss
C0270984  |  metabolic myopathy
C0235031  |  neurologic symptoms
C0221163  |  motor disorders
C0036572  |  seizures
C0029132  |  optic neuropathy
C0026848  |  myopathy
C0026755  |  multiple carboxylase deficiency
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:2)
C0029132  |  optic neuropathy  |  1
C0036572  |  seizures  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:159)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs104893686NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645063TG
rs104893687NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635614CT
rs104893688NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645451CT
rs1048936889654207686BTDumls:C0220754UNIPROTPartial biotinidase deficiency is usually due to the D444H mutation in the biotinidase gene.0.5746117111998BTD315645451CT
rs104893692NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645322AC
rs112195009NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644488GA
rs119103232NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635479GA
rs1307313910206677686BTDumls:C0220754UNIPROTWe have identified two new mutations in exon D of the biotinidase gene of children with profound biotinidase deficiency ascertained by newborn screening.0.5746117111998BTD315644367GA
rs13073139NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644367GA
rs1307888110206677686BTDumls:C0220754UNIPROTWe have identified two new mutations in exon D of the biotinidase gene of children with profound biotinidase deficiency ascertained by newborn screening.0.5746117111998BTD315645186GC
rs13078881NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645186GC
rs138818907NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645345CT
rs146011150NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635507AG
rs146015592NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644326GA
rs146136265NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645485CA
rs146600671NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645225GA
rs151071780NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635641CG,T
rs181396238NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645288GA,C
rs190386869NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644499CG,T
rs200327983NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644902AC
rs200337373NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644520GA,C
rs201023772NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645061AG
rs201604102NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645311CG
rs28934601NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644611AG
rs34885143NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635512GA
rs35034250NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645027CT
rs35145938NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645140CA,T
rs35976361NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644736AG
rs367902696NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315642041GA
rs372844636NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644487CT
rs374141881NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645093GA
rs374681173NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315642052AC,G
rs375712490NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315641939GT
rs377651057NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644791GA
rs397507170NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635563GA,T
rs397507171NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635624CA,T
rs397507172NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315641924TG
rs397507173NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644415CT
rs397507174NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644485AG
rs397507175NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644590GA
rs397507176NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644824AG
rs397514333NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635591TC
rs397514334NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644721GC
rs397514335NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645127GA,C
rs397514336NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635515GT
rs397514337NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635538CA,T
rs397514338NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635539GA,T
rs397514339NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635550TG
rs397514340NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635569GA
rs397514341NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635573AG
rs397514343NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635615GA
rs397514345NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645217AC,G
rs397514346NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635625CTTGGAGCT-
rs397514347NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635627TC
rs397514348NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635657AG
rs397514349NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635662CT
rs397514350NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635677GA
rs397514351NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315641908GT
rs397514352NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315641932GA,C
rs397514353NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315641954AG
rs397514354NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315641962AG
rs397514355NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315641980TG
rs397514356NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315641991C-
rs397514357NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315642022CA
rs397514359NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315642043TC
rs397514360NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315642057GA
rs397514362NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644322CT
rs397514363NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644325CT
rs397514364NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644341CT
rs397514365NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644346AG-
rs397514366NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644371AG
rs397514367NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644384GT
rs397514368NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644400A-
rs397514369NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644413GA
rs397514370NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644439AG
rs397514371NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644440AG
rs397514372NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644443CG
rs397514373NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644450CGT-
rs397514374NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644450C-
rs397514375NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644451GA
rs397514376NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644461AG,T
rs397514377NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644497AG
rs397514378NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644508GC
rs397514379NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644510GA,C
rs397514380NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644538GT
rs397514381NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644565GA
rs397514382NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644599TC
rs397514383NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644613CT
rs397514384NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644620TC
rs397514385NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644650AT
rs397514386NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644789TG
rs397514387NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644670TG
rs397514388NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644688CG
rs397514389NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644689TC
rs397514390NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644692TG
rs397514391NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644743TG
rs397514392NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644752CT
rs397514393NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644785GA
rs397514394NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644788GA
rs397514395NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644789T-
rs397514396NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644790GA
rs397514397NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644905C-
rs397514398NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644908C-
rs397514399NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644952TC
rs397514400NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644962CT
rs397514401NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645013GA
rs397514402NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645190GT
rs397514403NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645047GA-
rs397514404NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645095CTATCTCCACGT-
rs397514405NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645067CT
rs397514406NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645070TC
rs397514407NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645095C-
rs397514408NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645108TC
rs397514409NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645105GT
rs397514410NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645109GC
rs397514411NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645120-C
rs397514412NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645123TC
rs397514413NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645124GC
rs397514414NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645131TG
rs397514415NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645169AG
rs397514416NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645170TA
rs397514417NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645189GA
rs397514418NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645195CT
rs397514419NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645208GA
rs397514420NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645240A-
rs397514421NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645244GA
rs397514422NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645315TC
rs397514423NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645315T-
rs397514424NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645319GA
rs397514425NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645349-T
rs397514426NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645367TA
rs397514427NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645387CG
rs397514428NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645466GA
rs397514429NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645469GA
rs397514430NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645472-T
rs397514431NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645475AG
rs397514432NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645483GC
rs397514433NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644857TA
rs397514434NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645014GA
rs397514436NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635571GC
rs397514437NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644374TG
rs397514438NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644614CT
rs397514439NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315642005-A
rs397514440NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645250-G
rs398123138NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645364GGATG-
rs398123139NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644482GA
rs587783002NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635636TG
rs587783003NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315642053CG,T
rs587783004NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644539AG
rs587783005NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644557CT
rs587783006NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315644754AC
rs587783007NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645228-T
rs587783008NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315641893T-
rs672601248NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645083GGGAAAGGAAGGCTANNNNNNNNNNN,TTCCAATGGCC
rs786204672NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635584-ATCC
rs80338684NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315635477GCGGCTGTCC
rs80338685NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645224AC
rs803386859654207686BTDumls:C0220754UNIPROTPartial biotinidase deficiency is usually due to the D444H mutation in the biotinidase gene.0.5746117111998BTD315645224AC
rs80338686NA686BTDumls:C0220754CLINVARNA0.574611711NABTD315645468CA,T
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0000407Sensorineural hearing impairmentMP:0006330syndromic hearing impairment;HP:0000648Optic atrophy
Mapped by homologous gene(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0001992Organic aciduriaMP:0004185abnormal adipocyte glucose uptake;HP:0000365Hearing impairment
Chemical(Total Drugs:0)
(Waiting for update.)
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