All categories LOINC
MeSH NDFRT
CSP AOD LCH
NCI RXNORM
USPMG VANDF
MEDLINEPLUS CST
HL7V2.5 HL7V3.0
UWDA PDQ HUGO
ICD9CM ICD10
OMIM SRC GO
COSTAR DXP QMR
NCBI CCS SPN
AIR PNDS RAM
AOT MCM HCPCS
     +ICPC      +MTH

home

UMLS

Lobstein`s syndrome

Lobstein`s Disease

C0023931    ENG (English)     MSH (Medical Subject Headings )

Disease, Lobstein

C0023931    ENG (English)     MSH (Medical Subject Headings )

Lobstein Disease

C0023931    ENG (English)     MSH (Medical Subject Headings )

Lobsteins Disease

C0023931    ENG (English)     MSH (Medical Subject Headings )

Disease, Lobstein`s

C0023931    ENG (English)     MSH (Medical Subject Headings )

Lobstein disease

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Lobstein disease

C0023931    ENG (English)     SNMI (SNOMED Intl )

Osteogenesis Imperfecta Tarda

C0023931    ENG (English)     MSH (Medical Subject Headings )

Osteogenesis imperfecta tarda

C0023931    ENG (English)     SNMI (SNOMED Intl )

Osteogenesis imperfecta tarda

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Osteogenesis imperfecta tarda

C0023931    ENG (English)     SNM (SNOMED )

osteogenesis imperfecta tarda

C0023931    ENG (English)     CHV

Osteogenesis Imperfecta Tardas

C0023931    ENG (English)     MSH (Medical Subject Headings )

OSTEOGENESIS IMPERFECTA TARDA

C0023931    ENG (English)     OMIM

Osteogenesis Imperfecta with Blue Sclerae

C0023931    ENG (English)     MSH (Medical Subject Headings )

OSTEOGENESIS IMPERFECTA WITH BLUE SCLERAE

C0023931    ENG (English)     OMIM

Osteogenesis imperfecta with blue sclerae

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Osteogenesis imperfecta with blue sclerae

C0023931    ENG (English)     SNMI (SNOMED Intl )

OI type 1

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

OI type 1

C0023931    ENG (English)     SNMI (SNOMED Intl )

Adair-Dighton syndrome

C0023931    ENG (English)     SNM (SNOMED )

Adair-Dighton syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Adair-Dighton syndrome

C0023931    ENG (English)     SNMI (SNOMED Intl )

Fragilitas ossium-blue sclerae-otosclerosis syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Fragilitas ossium-blue sclerae-otosclerosis syndrome

C0023931    ENG (English)     SNMI (SNOMED Intl )

Blue sclerae syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Blue sclerae syndrome

C0023931    ENG (English)     SNMI (SNOMED Intl )

van der Hoeve syndrome with deafness

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

van der Hoeve syndrome with deafness

C0023931    ENG (English)     SNMI (SNOMED Intl )

Spurway-Eddowes syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Spurway-Eddowes syndrome

C0023931    ENG (English)     SNMI (SNOMED Intl )

Eddowes syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Eddowes syndrome

C0023931    ENG (English)     SNMI (SNOMED Intl )

Ekman-Lobstein syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Ekman-Lobstein syndrome

C0023931    ENG (English)     SNMI (SNOMED Intl )

Ekman syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Ekman syndrome

C0023931    ENG (English)     SNMI (SNOMED Intl )

Fragilitas ossium hereditaria tarda

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Fragilitas ossium hereditaria tarda

C0023931    ENG (English)     SNMI (SNOMED Intl )

Osteogenesis imperfecta type I

C0023931    ENG (English)     RCD (Read Codes)

Osteogenesis imperfecta type I

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Osteogenesis imperfecta, type I

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Osteogenesis imperfecta, type I

C0023931    ENG (English)     SNMI (SNOMED Intl )

i imperfecta osteogenesis type

C0023931    ENG (English)     CHV

OSTEOGENESIS IMPERFECTA, TYPE I

C0023931    ENG (English)     OMIM

osteogenesis imperfecta type I

C0023931    ENG (English)     MEDCIN

Osteopsathyrosis idiopathica tarda

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Osteopsathyrosis idiopathica tarda

C0023931    ENG (English)     SNMI (SNOMED Intl )

Osteogenesis imperfecta psathyrotica

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Osteogenesis imperfecta psathyrotica

C0023931    ENG (English)     SNMI (SNOMED Intl )

Van der Hoeve`s syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Van der Hoeve`s syndrome

C0023931    ENG (English)     SNM (SNOMED )

Osteogenesis imperfecta with blue sclerae (disorder)

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Osteogenesis imperfecta type I (disorder)

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Eddowe`s syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Lobstein`s syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Van der Hoeve

C0023931    ENG (English)     ICPC2ICD10ENG

Lobstein

C0023931    ENG (English)     ICPC2ICD10ENG

LOBSTEIN DIS

C0023931    ENG (English)     MSH (Medical Subject Headings )

LOBSTEINS DIS

C0023931    ENG (English)     MSH (Medical Subject Headings )

OI, TYPE I

C0023931    ENG (English)     OMIM

OI1

C0023931    ENG (English)     OMIM

osteogenesis imperfecta type I (diagnosis)

C0023931    ENG (English)     MEDCIN

Osteogenesis Imperfecta, Type 1

C0023931    ENG (English)     MSH (Medical Subject Headings )

Maladie de Lobstein

C0023931    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Ostéopsathyrose

C0023931    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Ostéogenèse imparfaite tardive

C0023931    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Lobstein-Krankheit

C0023931    GER (German)     MSHGER (Medical Subject Headings German Language Edition )

Osteopsathyrosis Lobstein

C0023931    GER (German)     MSHGER (Medical Subject Headings German Language Edition )

Doença de Lobstein

C0023931    POR (Portuguese)     MSHPOR (Medical Subject Headings Portuguese Language Edition )

osteogénesis imperfecta tipo I

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Enfermedad de Lobstein

C0023931    SPA (Spanish)     MSHSPA (Medical Subject Headings Spanish Language Edition )

enfermedad de Lobstein

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

fragilidad ósea hereditaria tardía

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

osteogenia imperfecta con esclerótica azul

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

osteogenia imperfecta con esclerótica azul (trastorno)

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

osteogenia imperfecta tardía

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

osteogenia imperfecta tipo I

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

osteogénesis imperfecta tipo I (trastorno)

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de Adair - Dighton

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de Ekman

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de Ekman - Lobstein

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de Spurway - Eddowes

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de escleróticas azules

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de fragilidad ósea, esclerótica azul, otosclerosis

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de van der Hoeve con sordera

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Adair-Dighton syndrome

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Eddowe`s syndrome

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

(Osteogenesis imperfecta) or (Vrolik`s disease) or (syndromes: [Adair-Dighton] or [Lobstein`s] or [Van der Hoeve`s])

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Van der Hoeve`s syndrome

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Lobstein`s syndrome

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Lobstein`s Disease

C0023931    ENG (English)     MSH (Medical Subject Headings )

Disease, Lobstein

C0023931    ENG (English)     MSH (Medical Subject Headings )

Lobstein Disease

C0023931    ENG (English)     MSH (Medical Subject Headings )

Lobsteins Disease

C0023931    ENG (English)     MSH (Medical Subject Headings )

Disease, Lobstein`s

C0023931    ENG (English)     MSH (Medical Subject Headings )

Lobstein disease

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Lobstein disease

C0023931    ENG (English)     SNMI (SNOMED Intl )

Osteogenesis Imperfecta Tarda

C0023931    ENG (English)     MSH (Medical Subject Headings )

Osteogenesis imperfecta tarda

C0023931    ENG (English)     SNMI (SNOMED Intl )

Osteogenesis imperfecta tarda

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Osteogenesis imperfecta tarda

C0023931    ENG (English)     SNM (SNOMED )

osteogenesis imperfecta tarda

C0023931    ENG (English)     CHV

Osteogenesis Imperfecta Tardas

C0023931    ENG (English)     MSH (Medical Subject Headings )

OSTEOGENESIS IMPERFECTA TARDA

C0023931    ENG (English)     OMIM

Osteogenesis Imperfecta with Blue Sclerae

C0023931    ENG (English)     MSH (Medical Subject Headings )

OSTEOGENESIS IMPERFECTA WITH BLUE SCLERAE

C0023931    ENG (English)     OMIM

Osteogenesis imperfecta with blue sclerae

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Osteogenesis imperfecta with blue sclerae

C0023931    ENG (English)     SNMI (SNOMED Intl )

OI type 1

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

OI type 1

C0023931    ENG (English)     SNMI (SNOMED Intl )

Adair-Dighton syndrome

C0023931    ENG (English)     SNM (SNOMED )

Adair-Dighton syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Adair-Dighton syndrome

C0023931    ENG (English)     SNMI (SNOMED Intl )

Fragilitas ossium-blue sclerae-otosclerosis syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Fragilitas ossium-blue sclerae-otosclerosis syndrome

C0023931    ENG (English)     SNMI (SNOMED Intl )

Blue sclerae syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Blue sclerae syndrome

C0023931    ENG (English)     SNMI (SNOMED Intl )

van der Hoeve syndrome with deafness

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

van der Hoeve syndrome with deafness

C0023931    ENG (English)     SNMI (SNOMED Intl )

Spurway-Eddowes syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Spurway-Eddowes syndrome

C0023931    ENG (English)     SNMI (SNOMED Intl )

Eddowes syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Eddowes syndrome

C0023931    ENG (English)     SNMI (SNOMED Intl )

Ekman-Lobstein syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Ekman-Lobstein syndrome

C0023931    ENG (English)     SNMI (SNOMED Intl )

Ekman syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Ekman syndrome

C0023931    ENG (English)     SNMI (SNOMED Intl )

Fragilitas ossium hereditaria tarda

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Fragilitas ossium hereditaria tarda

C0023931    ENG (English)     SNMI (SNOMED Intl )

Osteogenesis imperfecta type I

C0023931    ENG (English)     RCD (Read Codes)

Osteogenesis imperfecta type I

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Osteogenesis imperfecta, type I

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Osteogenesis imperfecta, type I

C0023931    ENG (English)     SNMI (SNOMED Intl )

i imperfecta osteogenesis type

C0023931    ENG (English)     CHV

OSTEOGENESIS IMPERFECTA, TYPE I

C0023931    ENG (English)     OMIM

osteogenesis imperfecta type I

C0023931    ENG (English)     MEDCIN

Osteopsathyrosis idiopathica tarda

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Osteopsathyrosis idiopathica tarda

C0023931    ENG (English)     SNMI (SNOMED Intl )

Osteogenesis imperfecta psathyrotica

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Osteogenesis imperfecta psathyrotica

C0023931    ENG (English)     SNMI (SNOMED Intl )

Van der Hoeve`s syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Van der Hoeve`s syndrome

C0023931    ENG (English)     SNM (SNOMED )

Osteogenesis imperfecta with blue sclerae (disorder)

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Osteogenesis imperfecta type I (disorder)

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Eddowe`s syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Lobstein`s syndrome

C0023931    ENG (English)     SNM (SNOMED Clinical Terms )

Van der Hoeve

C0023931    ENG (English)     ICPC2ICD10ENG

Lobstein

C0023931    ENG (English)     ICPC2ICD10ENG

LOBSTEIN DIS

C0023931    ENG (English)     MSH (Medical Subject Headings )

LOBSTEINS DIS

C0023931    ENG (English)     MSH (Medical Subject Headings )

OI, TYPE I

C0023931    ENG (English)     OMIM

OI1

C0023931    ENG (English)     OMIM

osteogenesis imperfecta type I (diagnosis)

C0023931    ENG (English)     MEDCIN

Osteogenesis Imperfecta, Type 1

C0023931    ENG (English)     MSH (Medical Subject Headings )

Maladie de Lobstein

C0023931    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Ostéopsathyrose

C0023931    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Ostéogenèse imparfaite tardive

C0023931    FRE (French)     MSHFRE (Medical Subject Headings French Language Edition )

Lobstein-Krankheit

C0023931    GER (German)     MSHGER (Medical Subject Headings German Language Edition )

Osteopsathyrosis Lobstein

C0023931    GER (German)     MSHGER (Medical Subject Headings German Language Edition )

Doença de Lobstein

C0023931    POR (Portuguese)     MSHPOR (Medical Subject Headings Portuguese Language Edition )

osteogénesis imperfecta tipo I

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Enfermedad de Lobstein

C0023931    SPA (Spanish)     MSHSPA (Medical Subject Headings Spanish Language Edition )

enfermedad de Lobstein

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

fragilidad ósea hereditaria tardía

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

osteogenia imperfecta con esclerótica azul

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

osteogenia imperfecta con esclerótica azul (trastorno)

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

osteogenia imperfecta tardía

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

osteogenia imperfecta tipo I

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

osteogénesis imperfecta tipo I (trastorno)

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de Adair - Dighton

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de Ekman

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de Ekman - Lobstein

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de Spurway - Eddowes

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de escleróticas azules

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de fragilidad ósea, esclerótica azul, otosclerosis

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

síndrome de van der Hoeve con sordera

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Adair-Dighton syndrome

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Eddowe`s syndrome

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

(Osteogenesis imperfecta) or (Vrolik`s disease) or (syndromes: [Adair-Dighton] or [Lobstein`s] or [Van der Hoeve`s])

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Van der Hoeve`s syndrome

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )

Lobstein`s syndrome

C0023931    SPA (Spanish)     SCTSPA (SNOMED Clinical Terms, Spanish Language Edition )


Buy medical website. Electronic digital document management. $250-$500 /yearly