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ALG3-CDG
ORPHA:79321CID-10 · E77.8CID-11 · 5C54.0OMIM 601110DOENÇA RARA
Esta doença tem causa genética. Recomendamos procurar um médico geneticista para diagnóstico, exames genéticos e aconselhamento familiar.
Visão / ocularInício neonatalHerança AR
Sinônimos clínicos: Doença congénita da glicosilação tipo 1d · Síndrome CDG tipo Id · CDG1D · +4

É um tipo de doença congênita (de nascença) que afeta um processo importante no corpo chamado glicosilação N-ligada. É caracterizada por problemas neurológicos sérios, como fraqueza muscular (hipotonia), atraso no desenvolvimento, deficiência intelectual, cabeça menor que o normal que aparece depois do nascimento (microcefalia pós-natal), e uma perda progressiva de massa no cérebro e no cerebelo. É comum que a pessoa tenha epilepsia, frequentemente com um padrão específico de atividade elétrica no cérebro (hipsarritmia). Outras características que podem ser observadas incluem: dificuldade de ganhar peso e crescer adequadamente, rigidez em várias articulações desde o nascimento (artrogripose múltipla congênita ou AMC), problemas de visão (como perda do nervo óptico e uma fenda na parte colorida do olho, chamada coloboma de íris) e características faciais distintas, como olhos mais afastados com a parte superior do nariz mais larga, orelhas grandes e grossas, lábios finos e queixo pequeno (micrognatia). A doença é causada por alterações (mutações) no gene ALG3 (localizado na posição 3q27.3) que fazem com que ele não funcione corretamente.

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Introdução

O que você precisa saber de cara

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EM LINGUAGEM SIMPLES

A ALG3-CDG é uma doença genética muito rara presente desde o nascimento, que afeta a montagem adequada de proteínas no organismo. Ela costuma causar atraso importante no desenvolvimento da criança, fraqueza muscular, problemas de visão e crises convulsivas precoces. A condição não tem cura nem remédios específicos que a corrijam diretamente, mas os cuidados focam em tratar as queixas e complicações. No SUS, a doença não conta com PCDT próprio nem remédios específicos na farmácia pública, mas disponibiliza exames diagnósticos e atendimento em reabilitação para doenças raras.

📋
Informacoes curadas por IA — podem conter imprecisoes

É um tipo de doença congênita (de nascença) que afeta um processo importante no corpo chamado glicosilação N-ligada. É caracterizada por problemas neurológicos sérios, como fraqueza muscular (hipotonia), atraso no desenvolvimento, deficiência intelectual, cabeça menor que o normal que aparece depois do nascimento (microcefalia pós-natal), e uma perda progressiva de massa no cérebro e no cerebelo. É comum que a pessoa tenha epilepsia, frequentemente com um padrão específico de atividade elétrica no cérebro (hipsarritmia). Outras características que podem ser observadas incluem: dificuldade de ganhar peso e crescer adequadamente, rigidez em várias articulações desde o nascimento (artrogripose múltipla congênita ou AMC), problemas de visão (como perda do nervo óptico e uma fenda na parte colorida do olho, chamada coloboma de íris) e características faciais distintas, como olhos mais afastados com a parte superior do nariz mais larga, orelhas grandes e grossas, lábios finos e queixo pequeno (micrognatia). A doença é causada por alterações (mutações) no gene ALG3 (localizado na posição 3q27.3) que fazem com que ele não funcione corretamente.

Publicações científicas
21 artigos
Último publicado: 2025 Dec

Escala de raridade

CLASSIFICAÇÃO ORPHANET · BRASIL 2024
<1 / 1 000 000
Ultra-rara
<1/50k
Muito rara
1/20k
Rara
1/10k
Pouco freq.
1/5k
Incomum
1/2k
Prevalência
0.0
Worldwide
Casos conhecidos
15
pacientes catalogados
Início
Infancy
+ neonatal
🏥
SUS: Cobertura mínimaScore: 15%
6 procedimentos SIGTAPCID-10: E77.8
🇧🇷Dados SUS / DATASUS
EXAMES E PROCEDIMENTOS RELACIONADOS (6)
•
Dosagem de aminoácidos (erros inatos)
•
Dosagem de ácidos orgânicos na urina
•
Teste de triagem para erros inatos do metabolismo
•
Sequenciamento completo do exoma (WES)
•
Teste do pezinho (triagem neonatal)
•
Atendimento em reabilitação — doenças raras
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Entender a doença

Do básico ao detalhe, leia no seu ritmo

Preparando trilha educativa...

Sinais e sintomas

O que aparece no corpo e com que frequência cada sintoma acontece

Partes do corpo afetadas

🧠
Neurológico
13 sintomas
🦴
Ossos e articulações
9 sintomas
👁️
Olhos
8 sintomas
😀
Face
7 sintomas
💪
Músculos
4 sintomas
🫃
Digestivo
4 sintomas

+ 18 sintomas em outras categorias

Características mais comuns

100%prev.
HP:0003577
Obrigatório (100%)
100%prev.
Atrofia óptica
Obrigatório (100%)
100%prev.
Perfil de isoforma de transferrina tipo I
Obrigatório (100%)
100%prev.
Atraso global do desenvolvimento
Muito frequente (99-80%)
100%prev.
Tetraparesia espástica
Ocasional (29-5%)
100%prev.
Convulsão
Frequente (79-30%)
78sintomas
Muito frequente (13)
Frequente (12)
Ocasional (6)
Muito raro (17)
Sem dados (30)

Os sintomas variam de pessoa para pessoa. Abaixo estão as 78 características clínicas mais associadas, ordenadas por frequência.

Obrigatório (100%)100%
Atrofia ópticaOptic atrophy
Obrigatório (100%)100%
Perfil de isoforma de transferrina tipo IType I transferrin isoform profile
Obrigatório (100%)100%
Atraso global do desenvolvimentoGlobal developmental delay
Muito frequente (99-80%)100%
Tetraparesia espásticaSpastic tetraparesis
Ocasional (29-5%)100%

Linha do tempo da pesquisa

Publicações por ano — veja quando o interesse científico cresceu
Anos de pesquisa1desde 2025
Total histórico21PubMed
Últimos 10 anos19publicações
Pico20215 papers
Linha do tempo
2025Hoje · 2026📈 2021Ano de pico
Publicações por ano (últimos 10 anos)

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Genética e causas

O que está alterado no DNA e como passa nas famílias

Genes associados

1 gene identificado com associação a esta condição. Padrão de herança: Autosomal recessive.

Curadoria gene-doença

fontes oficiais
ALG3
ALG3
ALG3Dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferaseDisease-causing germline mutation(s) (loss of function) inTolerante
VIAS BIOLÓGICAS (1)
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein
MECANISMO DE DOENÇA

Congenital disorder of glycosylation 1D

A form of congenital disorder of glycosylation, a multisystem disorder caused by a defect in glycoprotein biosynthesis and characterized by under-glycosylated serum glycoproteins. Congenital disorders of glycosylation result in a wide variety of clinical features, such as defects in the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions.

OUTRAS DOENÇAS (1)
ALG3-congenital disorder of glycosylation
HGNC:23056UniProt:Q92685

Variantes genéticas (ClinVar)

109 variantes patogênicas registradas no ClinVar.

🧬 ALG3: NM_005787.6(ALG3):c.606-2A>C ()
🧬 ALG3: NM_005787.6(ALG3):c.859C>T (p.Arg287Ter) ()
🧬 ALG3: GRCh37/hg19 3q22.1-29(chr3:132561657-197851986)x3 ()
🧬 ALG3: NM_005787.6(ALG3):c.452C>T (p.Pro151Leu) ()
🧬 ALG3: NM_005787.6(ALG3):c.1162del (p.Val388fs) ()
Ver todas no ClinVar

Diagnóstico

Os sinais que médicos procuram e os exames que confirmam

Carregando...

Tratamento e manejo

Remédios, cuidados de apoio e o que precisa acompanhar

Carregando informações de tratamento...

Onde tratar no SUS

Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)

🇧🇷 Atendimento SUS — ALG3-CDG

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Selecione um estado ou use sua localização para ver resultados.

Dados de DATASUS/CNES, SBGM, ABNeuro e Ministério da Saúde. Sempre confirme a disponibilidade diretamente com o estabelecimento.

Pesquisa ativa

Ensaios clínicos abertos e novidades científicas recentes

Pesquisa e ensaios clínicos

Nenhum ensaio clínico registrado para esta condição.

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Publicações mais relevantes

🥉Melhor nível de evidência: Relato de caso
Timeline de publicações
19 papers (10 anos)
#1

First case report of effective and safe application of cannabidiol to treat concurrent ALG3-CDG and Lennox-Gastaut Syndrome.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2025 Apr

This study presents the first reported case of a Korean patient with Alpha-1,3-Mannosyltransferase-Congenital Disorder of Glycosylation (ALG3-CDG), characterized by a novel maternally inherited missense mutation and a previously reported paternally inherited nonsense mutation. The patient exhibited typical ALG3-CDG manifestations, including developmental delays, epilepsy, and multisystem involvement, alongside a diagnosis of Lennox-Gastaut Syndrome (LGS). Cannabidiol therapy, combined with dietary management, led to seizure freedom for over 13 months, significant EEG improvement, and enhanced developmental outcomes. This case underscores the potential of cannabidiol as a promising treatment strategy for patients with ALG3-CDG and refractory epilepsy, broadening therapeutic perspectives for this rare disorder.

#2

Insights into ALG3-CDG: A case study combining glycan profiling and genetic analysis.

Molecular genetics and metabolism reports2025 Dec

Congenital disorders of glycosylation (CDG) are a group of rare metabolic disorders caused by the defects in the glycosylation pathways of biomacromolecules leading to altered glycoprofiles in affected individuals. In this case study, we present a 3-year-old Slovak male patient with developmental delay, hearing impairment, epilepsy, microcephaly, facial dysmorphism, corpus callosum dysgenesis, and cardiac abnormalities. To elucidate the underlying cause, we performed LC-ESI-MS analysis of RapiFluor-labelled N-glycans released from blood serum glycoproteins. The results revealed an abnormal N-glycan profile, characterized by an increased relative abundance of truncated mannosylated structures (Hex3HexNAc2 and Hex4HexNAc2) and a decreased presence of higher-order mannose structures (Hex6-8HexNAc2). A molecular analysis was also conducted. Whole exome sequencing confirmed a diagnosis of ALG3-CDG with compound heterozygous variants: c.165C > T (p.Gly55=) and c.1060C > T (p.Arg354Cys) in the ALG3 gene, encoding alpha-1,3-mannosyltransferase in the endoplasmic reticulum. This presented case highlights the importance of glycan profiling and genetic analysis in diagnosing congenital disorders of glycosylation, facilitating early intervention and management.

#3

Deficient glycan extension and endoplasmic reticulum stresses in ALG3-CDG.

Journal of inherited metabolic disease2024 Jul

ALG3-CDG is a rare congenital disorder of glycosylation (CDG) with a clinical phenotype that includes neurological manifestations, transaminitis, and frequent infections. The ALG3 enzyme catalyzes the first step of endoplasmic reticulum (ER) luminal glycan extension by adding mannose from Dol-P-Man to Dol-PP-Man5GlcNAc2 (Man5) forming Dol-PP-Man6. Such glycan extension is the first and fastest cellular response to ER stress, which is deficient in ALG3-CDG. In this study, we provide evidence that the unfolded protein response (UPR) and ER-associated degradation activities are increased in ALG3-CDG patient-derived cultured skin fibroblasts and there is constitutive activation of UPR mediated by the IRE1-α pathway. In addition, we show that N-linked Man3-4 glycans are increased in cellular glycoproteins and secreted plasma glycoproteins with hepatic or non-hepatic origin. We found that like other CDGs such as ALG1- or PMM2-CDG, in transferrin, the assembling intermediate Man5 in ALG3-CDG, are likely further processed into a distinct glycan, NeuAc1Gal1GlcNAc1Man3GlcNAc2, probably by Golgi mannosidases and glycosyltransferases. We predict it to be a mono-antennary glycan with the same molecular weight as the truncated glycan described in MGAT2-CDG. In summary, this study elucidates multiple previously unrecognized biochemical consequences of the glycan extension deficiency in ALG3-CDG which will have important implications in the pathogenesis of CDG.

#4

Cardiomyopathy, an uncommon phenotype of congenital disorders of glycosylation: Recommendations for baseline screening and follow-up evaluation.

Molecular genetics and metabolism2024 Aug

Congenital disorders of glycosylation (CDG) are a continuously expanding group of monogenic disorders that disrupt glycoprotein and glycolipid biosynthesis, leading to multi-systemic manifestations. These disorders are categorized into various groups depending on which part of the glycosylation process is impaired. The cardiac manifestations in CDG can significantly differ, not only across different types but also among individuals with the same genetic cause of CDG. Cardiomyopathy is an important phenotype in CDG. The clinical manifestations and progression of cardiomyopathy in CDG patients have not been well characterized. This study aims to delineate common patterns of cardiomyopathy across a range of genetic causes of CDG and to propose baseline screening and follow-up evaluation for this patient population. Patients with molecular confirmation of CDG who were enrolled in the prospective or memorial arms of the Frontiers in Congenital Disorders of Glycosylation Consortium (FCDGC) natural history study were ascertained for the presence of cardiomyopathy based on a retrospective review of their medical records. All patients were evaluated by clinical geneticists who are members of FCDGC at their respective academic centers. Patients were screened for cardiomyopathy, and detailed data were retrospectively collected. We analyzed their clinical and molecular history, imaging characteristics of cardiac involvement, type of cardiomyopathy, age at initial presentation of cardiomyopathy, additional cardiac features, the treatments administered, and their clinical outcomes. Of the 305 patients with molecularly confirmed CDG participating in the FCDGC natural history study as of June 2023, 17 individuals, nine females and eight males, were identified with concurrent diagnoses of cardiomyopathy. Most of these patients were diagnosed with PMM2-CDG (n = 10). However, cardiomyopathy was also observed in other diagnoses, including PGM1-CDG (n = 3), ALG3-CDG (n = 1), DPM1-CDG (n = 1), DPAGT1-CDG (n = 1), and SSR4-CDG (n = 1). All PMM2-CDG patients were reported to have hypertrophic cardiomyopathy. Dilated cardiomyopathy was observed in three patients, two with PGM1-CDG and one with ALG3-CDG; left ventricular non-compaction cardiomyopathy was diagnosed in two patients, one with PGM1-CDG and one with DPAGT1-CDG; two patients, one with DPM1-CDG and one with SSR4-CDG, were diagnosed with non-ischemic cardiomyopathy. The estimated median age of diagnosis for cardiomyopathy was 5 months (range: prenatal-27 years). Cardiac improvement was observed in three patients with PMM2-CDG. Five patients showed a progressive course of cardiomyopathy, while the condition remained unchanged in eight individuals. Six patients demonstrated pericardial effusion, with three patients exhibiting cardiac tamponade. One patient with SSR4-CDG has been recently diagnosed with cardiomyopathy; thus, the progression of the disease is yet to be determined. One patient with PGM1-CDG underwent cardiac transplantation. Seven patients were deceased, including five with PMM2-CDG, one with DPAGT1-CDG, and one with ALG3-CDG. Two patients died of cardiac tamponade from pericardial effusion; for the remaining patients, cardiomyopathy was not necessarily the primary cause of death. In this retrospective study, cardiomyopathy was identified in ∼6% of patients with CDG. Notably, the majority, including all those with PMM2-CDG, exhibited hypertrophic cardiomyopathy. Some cases did not show progression, yet pericardial effusions were commonly observed, especially in PMM2-CDG patients, occasionally escalating to life-threatening cardiac tamponade. It is recommended that clinicians managing CDG patients, particularly those with PMM2-CDG and PGM1-CDG, be vigilant of the cardiomyopathy risk and risk for potentially life-threatening pericardial effusions. Cardiac surveillance, including an echocardiogram and EKG, should be conducted at the time of diagnosis, annually throughout the first 5 years, followed by check-ups every 2-3 years if no concerns arise until adulthood. Subsequently, routine cardiac examinations every five years are advisable. Additionally, patients with diagnosed cardiomyopathy should receive ongoing cardiac care to ensure the effective management and monitoring of their condition. A prospective study will be required to determine the true prevalence of cardiomyopathy in CDG.

#5

Defective IGF-1 prohormone N-glycosylation and reduced IGF-1 receptor signaling activation in congenital disorders of glycosylation.

Cellular and molecular life sciences : CMLS2022 Feb 24

The insulin-like growth factor-1 (IGF-1) signaling pathway is crucial for the regulation of growth and development. The correct processing of the IGF-1Ea prohormone (proIGF-1Ea) and the IGF-1 receptor (IGF-1R) peptide precursor requires proper N-glycosylation. Deficiencies of N-linked glycosylation lead to a clinically heterogeneous group of inherited diseases called Congenital Disorders of Glycosylation (CDG). The impact of N-glycosylation defects on IGF-1/IGF-1R signaling components is largely unknown. In this study, using dermal fibroblasts from patients with different CDG [PMM2-CDG (n = 7); ALG3-CDG (n = 2); ALG8-CDG (n = 1); GMPPB-CDG (n = 1)], we analyzed the glycosylation pattern of the proIGF-1Ea, IGF-1 secretion efficiency and IGF-1R signaling activity. ALG3-CDG, ALG8-CDG, GMPPB-CDG and some PMM2-CDG fibroblasts showed hypoglycosylation of the proIGF-1Ea and lower IGF-1 secretion when compared with control (CTR). Lower IGF-1 serum concentration was observed in ALG3-CDG, ALG8-CDG and in some patients with PMM2-CDG, supporting our in vitro data. Furthermore, reduced IGF-1R expression level was observed in ALG3-CDG, ALG8-CDG and in some PMM2-CDG fibroblasts. IGF-1-induced IGF-1R activation was lower in most PMM2-CDG fibroblasts and was associated with decreased ERK1/2 phosphorylation as compared to CTR. In general, CDG fibroblasts showed a slight upregulation of Endoplasmic Reticulum (ER) stress genes compared with CTR, uncovering mild ER stress in CDG cells. ER-stress-related gene expression negatively correlated with fibroblasts IGF-1 secretion. This study provides new evidence of a direct link between N-glycosylation defects found in CDG and the impairment of IGF-1/IGF-1R signaling components. Further studies are warranted to determine the clinical consequences of reduced systemic IGF-1 availability and local activity in patients with CDG.

Publicações recentes

Ver todas no PubMed

📚 EuropePMC10 artigos no totalmostrando 19

2025

Insights into ALG3-CDG: A case study combining glycan profiling and genetic analysis.

Molecular genetics and metabolism reports
2025

First case report of effective and safe application of cannabidiol to treat concurrent ALG3-CDG and Lennox-Gastaut Syndrome.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
2024

Cardiomyopathy, an uncommon phenotype of congenital disorders of glycosylation: Recommendations for baseline screening and follow-up evaluation.

Molecular genetics and metabolism
2024

Deficient glycan extension and endoplasmic reticulum stresses in ALG3-CDG.

Journal of inherited metabolic disease
2022

Defective IGF-1 prohormone N-glycosylation and reduced IGF-1 receptor signaling activation in congenital disorders of glycosylation.

Cellular and molecular life sciences : CMLS
2021

Skeletal and Bone Mineral Density Features, Genetic Profile in Congenital Disorders of Glycosylation: Review.

Diagnostics (Basel, Switzerland)
2021

Prevalence of Congenital Disorders of Glycosylation in Childhood Epilepsy and Effects of Anti-Epileptic Drugs on the Transferrin Isoelectric Focusing Test.

Genes
2021

ALG3-CDG: a patient with novel variants and review of the genetic and ophthalmic findings.

BMC ophthalmology
2021

Expanding the phenotype, genotype and biochemical knowledge of ALG3-CDG.

Journal of inherited metabolic disease
2021

Clinical, biochemical and molecular phenotype of congenital disorders of glycosylation: long-term follow-up.

Orphanet journal of rare diseases
2020

ALG3-CDG: lethal phenotype and novel variants in Chinese siblings.

Journal of human genetics
2020

Successful treatment of intractable epilepsy with ketogenic diet therapy in twins with ALG3-CDG.

Brain &amp; development
2019

Novel variants and clinical symptoms in four new ALG3-CDG patients, review of the literature, and identification of AAGRP-ALG3 as a novel ALG3 variant with alanine and glycine-rich N-terminus.

Human mutation
2017

Congenital disorders of glycosylation: The Saudi experience.

American journal of medical genetics. Part A
2017

Phenotypic and genotypic spectrum of congenital disorders of glycosylation type I and type II.

Molecular genetics and metabolism
2017

Liver involvement in congenital disorders of glycosylation (CDG). A systematic review of the literature.

Journal of inherited metabolic disease
2016

Mitotic Intragenic Recombination: A Mechanism of Survival for Several Congenital Disorders of Glycosylation.

American journal of human genetics
2016

Electroclinical Features of Early-Onset Epileptic Encephalopathies in Congenital Disorders of Glycosylation (CDGs).

JIMD reports
2015

ALG3-CDG: Report of two siblings with antenatal features carrying homozygous p.Gly96Arg mutation.

American journal of medical genetics. Part A

Associações

Organizações que acompanham esta doença — pra ter apoio e orientação

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Doença com base genética

Um médico geneticista pode ajudar no diagnóstico de ALG3-CDG e no aconselhamento genético da família.

Vai consultar um especialista? Confirme o registro dele no conselho.
Conselhos e sociedades

Doenças relacionadas

Doenças com sintomas parecidos — ajudam quem ainda está buscando diagnóstico

Perguntas frequentes

O que as famílias mais perguntam sobre esta doença — cada resposta com a fonte de onde saiu

Respostas geradas por IA a partir das fontes citadas

É uma doença congênita rara do metabolismo causada pela falha na glicosilação N-ligada de proteínas. Ela é decorrente de mutações no gene ALG3 e afeta o desenvolvimento neurológico e físico desde a infância.

Referências

Fontes citadas no texto, publicações do grafo e bases de dados usadas neste verbete

5 publicações do grafo RarasNet (PubMed) · 7 bases de dados. Títulos, periódicos e PMIDs vêm direto da fonte, sem intermediação de IA.

  1. First case report of effective and safe application of cannabidiol to treat concurrent ALG3-CDG and Lennox-Gastaut Syndrome.
    Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2025PMID 39831946
  2. ORPHA:79321
    Orphanet
  3. GARD:9827
    GARD (NIH)
  4. Q66299820
    Wikidata

Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.

Citar este verbete

Raras. (s.d.). ALG3-CDG. Em Raras — Enciclopédia de Doenças Raras do Brasil. https://raras.org/doenca/alg3-cdg

Formato APA. Conteúdo sob CC BY 4.0 — reuso livre com atribuição.

Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar

Compêndio · Raras BR

ALG3-CDG

ORPHA:79321 · MONDO:0010998
🇧🇷 Brasil SUS
SIGTAP
6 procedimentos
Geral
Prevalência
<1 / 1 000 000
Casos
15 casos conhecidos
Herança
Autosomal recessive
CID-10
E77.8 · Outros distúrbios do metabolismo de glicoproteínas
CID-11
Início
Infancy, Neonatal
Prevalência
0.0 (Worldwide)
MedGen
UMLS
C1832736
EuropePMC
Wikidata
Papers 10a
Evidência
🥉 Relato de caso

📋 Origem dos dados

Esta página agrega dados de fontes públicas e oficiais. Dados sobre cobertura no SUS (PCDT, CEAF) são verificados ativamente por agente proativo (ver badge no infobox). Demais dados têm atribuição de fonte + data da última sincronização — clique para abrir o original.

Doença rara (ontologia)
fonte: Orphanet
Identificador unificado
fonte: MONDO
Genética mendeliana
fonte: OMIM
Indexação biomédica
fonte: MeSH (NLM)
Dado público estruturado
fonte: Wikidata
Rara