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anonychia-microcephaly syndrome - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

anonychia-microcephaly syndrome

MONDO:0011795

Also known as:Teebi-Kaurah syndromeanonychia total with microcephalyanonychia, total, with microcephaly

Overview

Anonychia-microcephaly syndrome is a multiple congenital anomaly disorder characterized by anonychia congenita totalis and microcephaly, and normal intelligence along with some minor anomalies including single transverse palmar creases, fifth-finger clinodactyly and widely-spaced teeth.

Diagnosis

Biomarker and diagnostic research for anonychia-microcephaly syndrome has been reported in the published literature.

Prognosis

Estimated prevalence: <1 in 1,000,000 (VERY_RARE).

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for anonychia-microcephaly syndrome.

203 publications have been identified in PubMed for anonychia-microcephaly syndrome. Kisho has analyzed 112 by research type. Research spans Review / Meta-Analysis (69%), Basic Science / Preclinical (17%), and Epidemiology / Natural History (6%).

Research Type	Count	% of Total
Research summaries	77	69%

Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 8:41 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:607214

Orphanet

European rare disease database

Orphanet:1094

GARD

Genetic and Rare Diseases Info Center

GARD:5123

Questions for Your Care Team

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anonychia-microcephaly syndrome

Overview

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

OMIM

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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