Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
Preferred Name

FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE

Synonyms

KUWAIT TYPE FACIODIGITOGENITAL SYNDROME

ID

http://purl.bioontology.org/ontology/OMIM/227330

altLabel

KUWAIT TYPE FACIODIGITOGENITAL SYNDROME

AARSKOG-LIKE SYNDROME

cui

C1856871

Has manifestation

http://purl.bioontology.org/ontology/OMIM/MTHU004811

http://purl.bioontology.org/ontology/OMIM/MTHU010545

http://purl.bioontology.org/ontology/OMIM/MTHU013069

http://purl.bioontology.org/ontology/OMIM/MTHU037446

http://purl.bioontology.org/ontology/OMIM/MTHU001627

http://purl.bioontology.org/ontology/OMIM/MTHU000504

http://purl.bioontology.org/ontology/OMIM/MTHU000579

http://purl.bioontology.org/ontology/OMIM/MTHU000506

http://purl.bioontology.org/ontology/OMIM/MTHU013066

http://purl.bioontology.org/ontology/OMIM/MTHU000229

http://purl.bioontology.org/ontology/OMIM/MTHU000231

http://purl.bioontology.org/ontology/OMIM/MTHU037444

http://purl.bioontology.org/ontology/OMIM/MTHU037448

http://purl.bioontology.org/ontology/OMIM/MTHU037450

http://purl.bioontology.org/ontology/OMIM/MTHU000512

http://purl.bioontology.org/ontology/OMIM/MTHU003105

http://purl.bioontology.org/ontology/OMIM/MTHU013072

http://purl.bioontology.org/ontology/OMIM/MTHU013070

http://purl.bioontology.org/ontology/OMIM/MTHU009600

http://purl.bioontology.org/ontology/OMIM/MTHU001511

http://purl.bioontology.org/ontology/OMIM/MTHU004091

http://purl.bioontology.org/ontology/OMIM/MTHU002002

http://purl.bioontology.org/ontology/OMIM/MTHU000191

http://purl.bioontology.org/ontology/OMIM/MTHU000848

http://purl.bioontology.org/ontology/OMIM/MTHU007320

http://purl.bioontology.org/ontology/OMIM/MTHU000066

http://purl.bioontology.org/ontology/OMIM/MTHU036626

http://purl.bioontology.org/ontology/OMIM/MTHU013067

http://purl.bioontology.org/ontology/OMIM/MTHU020487

http://purl.bioontology.org/ontology/OMIM/MTHU013068

http://purl.bioontology.org/ontology/OMIM/MTHU037445

http://purl.bioontology.org/ontology/OMIM/MTHU037443

http://purl.bioontology.org/ontology/OMIM/MTHU037449

http://purl.bioontology.org/ontology/OMIM/MTHU000088

http://purl.bioontology.org/ontology/OMIM/MTHU037447

http://purl.bioontology.org/ontology/OMIM/MTHU013065

http://purl.bioontology.org/ontology/OMIM/MTHU013071

http://purl.bioontology.org/ontology/OMIM/MTHU001853

http://purl.bioontology.org/ontology/OMIM/MTHU037451

http://purl.bioontology.org/ontology/OMIM/MTHU000189

http://purl.bioontology.org/ontology/OMIM/MTHU013073

http://purl.bioontology.org/ontology/OMIM/MTHU001852

http://purl.bioontology.org/ontology/OMIM/MTHU000263

http://purl.bioontology.org/ontology/OMIM/MTHU001946

http://purl.bioontology.org/ontology/OMIM/MTHU036366

MIMTYPEMEANING

Mendelian phenotype or locus, molecular basis unknown.

notation

227330

OMIM Entry Type

5

OMIM MimType Value

perc

prefLabel

FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE

tui

T047

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MESH/C535331 Medical Subject Headings CUI