MCID: HKF001
MIFTS: 7

Ho Kaufman Mcalister Syndrome

Categories: Bone diseases, Rare diseases

Aliases & Classifications for Ho Kaufman Mcalister Syndrome

MalaCards integrated aliases for Ho Kaufman Mcalister Syndrome:

Name: Ho Kaufman Mcalister Syndrome 52 71
Cleft Palate, Micrognathia, Wormian Bones, Congenital Heart Disease, Dislocated Hips, Absent Tibiae, Bowed Fibulae, Preaxial Polydactyly of the Feet, 52

Classifications:



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UMLS 71 C2931819

Summaries for Ho Kaufman Mcalister Syndrome

MalaCards based summary : Ho Kaufman Mcalister Syndrome, is also known as cleft palate, micrognathia, wormian bones, congenital heart disease, dislocated hips, absent tibiae, bowed fibulae, preaxial polydactyly of the feet,. Affiliated tissues include bone, heart and skin.

Wikipedia : 74 Ho-Kaufman-Mcalister syndrome, is a rare congenital malformation syndrome where infants are born with a... more...

Related Diseases for Ho Kaufman Mcalister Syndrome

Symptoms & Phenotypes for Ho Kaufman Mcalister Syndrome

Drugs & Therapeutics for Ho Kaufman Mcalister Syndrome

Search Clinical Trials , NIH Clinical Center for Ho Kaufman Mcalister Syndrome

Genetic Tests for Ho Kaufman Mcalister Syndrome

Anatomical Context for Ho Kaufman Mcalister Syndrome

MalaCards organs/tissues related to Ho Kaufman Mcalister Syndrome:

40
Bone, Heart, Skin

Publications for Ho Kaufman Mcalister Syndrome

Articles related to Ho Kaufman Mcalister Syndrome:

# Title Authors PMID Year
1
Congenital malformations. Cleft palate, congenital heart disease, absent tibiae, and polydactyly. 61
168764 1975

Variations for Ho Kaufman Mcalister Syndrome

Expression for Ho Kaufman Mcalister Syndrome

Search GEO for disease gene expression data for Ho Kaufman Mcalister Syndrome.

Pathways for Ho Kaufman Mcalister Syndrome

GO Terms for Ho Kaufman Mcalister Syndrome

Sources for Ho Kaufman Mcalister Syndrome

3 CDC
7 CNVD
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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
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41 MedGen
43 MeSH
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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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