MCID: RRH025
MIFTS: 4

Rare Hereditary Disease with Avascular Necrosis

Categories: Bone diseases, Rare diseases

Aliases & Classifications for Rare Hereditary Disease with Avascular Necrosis

MalaCards integrated aliases for Rare Hereditary Disease with Avascular Necrosis:

Name: Rare Hereditary Disease with Avascular Necrosis 58

Classifications:

Orphanet: 58  
Rare systemic and rhumatological diseases
Rare bone diseases


External Ids:

Orphanet 58 ORPHA399185

Summaries for Rare Hereditary Disease with Avascular Necrosis

MalaCards based summary : Rare Hereditary Disease with Avascular Necrosis Affiliated tissues include bone.

Related Diseases for Rare Hereditary Disease with Avascular Necrosis

Diseases in the Avascular Necrosis family:

Rare Hereditary Disease with Avascular Necrosis Secondary Avascular Necrosis
Primary Avascular Necrosis

Symptoms & Phenotypes for Rare Hereditary Disease with Avascular Necrosis

Drugs & Therapeutics for Rare Hereditary Disease with Avascular Necrosis

Search Clinical Trials , NIH Clinical Center for Rare Hereditary Disease with Avascular Necrosis

Genetic Tests for Rare Hereditary Disease with Avascular Necrosis

Anatomical Context for Rare Hereditary Disease with Avascular Necrosis

MalaCards organs/tissues related to Rare Hereditary Disease with Avascular Necrosis:

40
Bone

Publications for Rare Hereditary Disease with Avascular Necrosis

Variations for Rare Hereditary Disease with Avascular Necrosis

Expression for Rare Hereditary Disease with Avascular Necrosis

Search GEO for disease gene expression data for Rare Hereditary Disease with Avascular Necrosis.

Pathways for Rare Hereditary Disease with Avascular Necrosis

GO Terms for Rare Hereditary Disease with Avascular Necrosis

Sources for Rare Hereditary Disease with Avascular Necrosis

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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