Normal constitutional karyotype

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Normal constitutional karyotype" [OMIM:Normal constitutional karyotype]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY (OMIM:601347)