About the journal
Journal of Rare Diseases is an open-access journal published by Springer in Singapore, publishing in english. It is listed in DOAJ according to the sources read. Declared review time at DOAJ: 27 weeks. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Springer
- ISSN
- 2731-085X
- Country
- Singapore
- Languages
- english
- Access
- Open access
- Articles in DOAJ
- 185
- Declared review time
- 27 weeks
- Declared peer-review model
- peer_review
- Official website
- https://link.springer.com/journal/44162
Index listings
- DOAJ · 2024-06-25
- Indexing
- DOAJ
- APC
- —
- Declared review time (DOAJ)
- 27 weeks — journal-declared only (not measured)
- Activity (OpenAlex)
- Active — latest works 2026
- PublishLens list status
- Shown after sign-in
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- Choose your university and rank below ↓
Methodology signals (dated facts from their sources)
Details of the evaluation under the published methodology are shown to signed-in users (free).
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Descriptive metadata from public sources (DOAJ, OpenAlex, PubMed) as of the capture date shown — contains no assessment or judgment.
Articles in DOAJ
185
Most recent article
last month
Average review time (journal-declared via DOAJ)
27weeks
Works in OpenAlex
209
Last recorded publication year
2026
h-index
8
i10-index
7
From OpenAlex open data (CC0).
Editorial & policy12
- Last DOAJ review date
- 2026-03-17
- Added to DOAJ
- 2024-06-25
- Declared plagiarism screening
- Declared
- Other fees beyond APC
- No
- Declared digital preservation
- CLOCKSSPortico
- Observed digital preservation (Keepers registry)— snapshot 2026-09-21
- CLOCKSSPortico
- Editorial board
- Official page ↗
- Norwegian register (HK-dir)— 2026
- Level 1 — approved scholarly channel
- Open references deposited at Crossref
- 100%
- ORCID iDs in current deposits
- 53%
- Enrolled in Crossref Similarity Check
- ✓
- Deposits licence metadata at Crossref
- ✓
- Peer-review policy
- View policy
Identity & continuity2
- Source type
- journal
- NLM unique ID (PubMed)
- 9918522486706676
Classification2
Subjects (DOAJ)
LCC codes
Subject areas
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Lysosomal Storage Disorders Research
- Lysosomal Storage Disorders Research
- Mitochondrial Function and Pathology
- Health Systems, Economic Evaluations, Quality of Life
- Mitochondrial Function and Pathology
- Health Systems, Economic Evaluations, Quality of Life
Show all subjects (50)
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Connective tissue disorders research
- Parathyroid Disorders and Treatments
- Connective tissue disorders research
- Biomedical Research and Pathophysiology
- Genetic Syndromes and Imprinting
- Genetic Syndromes and Imprinting
- Parathyroid Disorders and Treatments
- Glycogen Storage Diseases and Myoclonus
- Glycogen Storage Diseases and Myoclonus
- Neonatal Health and Biochemistry
- Neonatal Health and Biochemistry
- Biomedical Research and Pathophysiology
- Genomic variations and chromosomal abnormalities
- Muscle Physiology and Disorders
- Genomic variations and chromosomal abnormalities
- Dermatological and Skeletal Disorders
- Muscle Physiology and Disorders
- Dermatological and Skeletal Disorders
- Neurogenetic and Muscular Disorders Research
- Neurogenetic and Muscular Disorders Research
- Congenital heart defects research
- Cellular transport and secretion
- Hemoglobinopathies and Related Disorders
- Genetic Neurodegenerative Diseases
- Genetic Neurodegenerative Diseases
- Medical Imaging and Pathology Studies
- Thyroid and Parathyroid Surgery
- Diabetes Treatment and Management
- Amino Acid Enzymes and Metabolism
- Genetics and Neurodevelopmental Disorders
- Craniofacial Disorders and Treatments
- Congenital heart defects research
- Diabetes Treatment and Management
- Amino Acid Enzymes and Metabolism
- Genetics and Neurodevelopmental Disorders
- Craniofacial Disorders and Treatments
- Thyroid and Parathyroid Surgery
- Genetic and rare skin diseases.
- Hemoglobinopathies and Related Disorders
- Cellular transport and secretion
Keywords (DOAJ)
- rare diseases
- genetic diseases
- oncology
- iinfectious diseases
- neurology
- immunology
Community confirmations — what users saw in MJL or Scopus Sources; not platform verification and never part of any score.
The journal's record in other sources:Web of Science MJLDOAJ