MEM
MCID: MLM001
MIFTS: 13

Milia, Multiple Eruptive (MEM)

Aliases & Classifications for Milia, Multiple Eruptive

MalaCards integrated aliases for Milia, Multiple Eruptive:

Name: Milia, Multiple Eruptive 57
Mem 57

Characteristics:

OMIM:

57
Inheritance:
autosomal dominant

Miscellaneous:
occurs from childhood to adulthood


HPO:

32
milia, multiple eruptive:
Inheritance autosomal dominant inheritance


External Ids:

OMIM 57 157400
MedGen 42 C0343079

Summaries for Milia, Multiple Eruptive

OMIM : 57 Multiple eruptive milia (MEM) is a rare condition in which clusters of milia (benign keratinous cysts) develop suddenly on the face and upper trunk (summary by Langley et al., 1997). (157400)

MalaCards based summary : Milia, Multiple Eruptive, also known as mem, is related to polykaryocytosis inducer and hydrocephalus. Related phenotype is milia.

Related Diseases for Milia, Multiple Eruptive

Diseases related to Milia, Multiple Eruptive via text searches within MalaCards or GeneCards Suite gene sharing:

(show top 50) (show all 67)
# Related Disease Score Top Affiliating Genes
1 polykaryocytosis inducer 10.2
2 hydrocephalus 10.2
3 congenital hydrocephalus 10.2
4 influenza 10.2
5 traumatic brain injury 10.2
6 pik3ca-related overgrowth syndrome 10.2
7 optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy 10.1
8 microvascular complications of diabetes 5 10.1
9 teratoma 10.1
10 movement disease 10.1
11 malignant teratoma 10.1
12 brain injury 10.1
13 breast cancer 9.9
14 hepatocellular carcinoma 9.9
15 multiple sclerosis 9.9
16 hand skill, relative 9.9
17 strabismus 9.9
18 triiodothyronine receptor auxiliary protein 9.9
19 hydatidiform mole, recurrent, 1 9.9
20 hydrocephalus, normal-pressure 9.9
21 neuroblastoma 1 9.9
22 pancreatic cancer 9.9
23 insulin-like growth factor i 9.9
24 arts syndrome 9.9
25 astigmatism 9.9
26 sickle cell anemia 9.9
27 schizophrenia 12 9.9
28 gastric cancer 9.9
29 leukemia, acute lymphoblastic 3 9.9
30 pachyonychia congenita 3 9.9
31 brain glioma 9.9
32 scoliosis 9.9
33 keratoconus 9.9
34 mumps 9.9
35 tetanus 9.9
36 heart disease 9.9
37 allergic hypersensitivity disease 9.9
38 hepatitis a 9.9
39 squamous cell papilloma 9.9
40 cholera 9.9
41 papilloma 9.9
42 kidney cancer 9.9
43 gliosarcoma 9.9
44 breast disease 9.9
45 gestational trophoblastic neoplasm 9.9
46 choriocarcinoma 9.9
47 ectomesenchymoma 9.9
48 schizoaffective disorder 9.9
49 eye disease 9.9
50 retinal disease 9.9

Graphical network of the top 20 diseases related to Milia, Multiple Eruptive:



Diseases related to Milia, Multiple Eruptive

Symptoms & Phenotypes for Milia, Multiple Eruptive

Human phenotypes related to Milia, Multiple Eruptive:

32
# Description HPO Frequency HPO Source Accession
1 milia 32 HP:0001056

Symptoms via clinical synopsis from OMIM:

57
Skin Nails Hair Skin:
eruptive milia (benign keratinous cysts on face and upper trunk)

Clinical features from OMIM:

157400

Drugs & Therapeutics for Milia, Multiple Eruptive

Search Clinical Trials , NIH Clinical Center for Milia, Multiple Eruptive

Genetic Tests for Milia, Multiple Eruptive

Anatomical Context for Milia, Multiple Eruptive

Publications for Milia, Multiple Eruptive

Articles related to Milia, Multiple Eruptive:

# Title Authors PMID Year
1
Multiple eruptive milia: report of a case, review of the literature, and a classification. 8
9270547 1997
2
[Multiple eruptive milia and striated leuconychia]. 8
4828151 1974
3
[Multiple eruptive milia-an organoid follicle hamartoma]. 8
13920696 1961

Variations for Milia, Multiple Eruptive

Expression for Milia, Multiple Eruptive

Search GEO for disease gene expression data for Milia, Multiple Eruptive.

Pathways for Milia, Multiple Eruptive

GO Terms for Milia, Multiple Eruptive

Sources for Milia, Multiple Eruptive

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 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 TGDB
71 Tocris
72 UMLS
73 UMLS via Orphanet
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