MCID: CRT027
MIFTS: 6

Cartwright Nelson Fryns Syndrome

Categories: Mental diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Cartwright Nelson Fryns Syndrome

MalaCards integrated aliases for Cartwright Nelson Fryns Syndrome:

Name: Cartwright Nelson Fryns Syndrome 54 74
Growth Retardation, Severe Mental Retardation, Acral Limb Deficiencies with Poorly Keratinized Nails 54

Classifications:



External Ids:

UMLS 74 C2931062

Summaries for Cartwright Nelson Fryns Syndrome

MalaCards based summary : Cartwright Nelson Fryns Syndrome, also known as growth retardation, severe mental retardation, acral limb deficiencies with poorly keratinized nails, is related to dwarfism.

Related Diseases for Cartwright Nelson Fryns Syndrome

Diseases related to Cartwright Nelson Fryns Syndrome via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 dwarfism 10.5

Symptoms & Phenotypes for Cartwright Nelson Fryns Syndrome

Drugs & Therapeutics for Cartwright Nelson Fryns Syndrome

Search Clinical Trials , NIH Clinical Center for Cartwright Nelson Fryns Syndrome

Genetic Tests for Cartwright Nelson Fryns Syndrome

Anatomical Context for Cartwright Nelson Fryns Syndrome

Publications for Cartwright Nelson Fryns Syndrome

Articles related to Cartwright Nelson Fryns Syndrome:

# Title Authors Year
1
Pre- and postnatal growth retardation--severe mental retardation--acral limb deficiencies with poorly keratinized nails. Another example of a distinct syndrome of inherited intrauterine dwarfism? ( 1801850 )
1991

Variations for Cartwright Nelson Fryns Syndrome

Expression for Cartwright Nelson Fryns Syndrome

Search GEO for disease gene expression data for Cartwright Nelson Fryns Syndrome.

Pathways for Cartwright Nelson Fryns Syndrome

GO Terms for Cartwright Nelson Fryns Syndrome

Sources for Cartwright Nelson Fryns Syndrome

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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