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 53 73
Growth Retardation, Severe Mental Retardation, Acral Limb Deficiencies with Poorly Keratinized Nails 53

Classifications:



External Ids:

UMLS 73 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 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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