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HPO → 對應的病歷用詞，並附加具此 HPO 的疾病作為參考。
Enamel hypoplasia
HP:0006297
對應病歷用詞(2)
具此 HPO 的疾病（附加參考）(45)
- 48,XYYY syndromeORPHA:99329 · Very frequent (99-80%)
- Microcephalic primordial dwarfism, Toriello typeORPHA:2643 · Very frequent (99-80%)
- Severe generalized junctional epidermolysis bullosaORPHA:79404 · Very frequent (99-80%)
- Steroid dehydrogenase deficiency-dental anomalies syndromeORPHA:3196 · Very frequent (99-80%)
- 17q11.2 microduplication syndromeORPHA:139474 · Frequent (79-30%)
- Amelogenesis imperfectaORPHA:88661 · Frequent (79-30%)
- Autoimmune polyendocrinopathy type 1ORPHA:3453 · Frequent (79-30%)
- Autosomal dominant generalized epidermolysis bullosa simplex, severe formORPHA:79396 · Frequent (79-30%)
- Cockayne syndromeORPHA:191 · Frequent (79-30%)
- Focal dermal hypoplasiaORPHA:2092 · Frequent (79-30%)
- Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndromeORPHA:363523 · Frequent (79-30%)
- Junctional epidermolysis bullosa inversaORPHA:79405 · Frequent (79-30%)
- Junctional epidermolysis bullosa with pyloric atresiaORPHA:79403 · Frequent (79-30%)
- Laryngo-onycho-cutaneous syndromeORPHA:2407 · Frequent (79-30%)
- Late-onset junctional epidermolysis bullosaORPHA:79406 · Frequent (79-30%)
- Localized junctional epidermolysis bullosaORPHA:251393 · Frequent (79-30%)
- Periodontal Ehlers-Danlos syndromeORPHA:75392 · Frequent (79-30%)
- Pfeiffer-Palm-Teller syndromeORPHA:2871 · Frequent (79-30%)
- Prader-Willi syndromeORPHA:739 · Frequent (79-30%)
- Pseudohypoparathyroidism type 1AORPHA:79443 · Frequent (79-30%)
- Pseudohypoparathyroidism type 1BORPHA:94089 · Frequent (79-30%)
- Pseudohypoparathyroidism type 1CORPHA:79444 · Frequent (79-30%)
- Regional odontodysplasiaORPHA:83450 · Frequent (79-30%)
- SCARF syndromeORPHA:3134 · Frequent (79-30%)
- Spondylocarpotarsal synostosisORPHA:3275 · Frequent (79-30%)
- Cockayne syndrome type 1ORPHA:90321 · Occasional (29-5%)
- Cockayne syndrome type 2ORPHA:90322 · Occasional (29-5%)
- Cockayne syndrome type 3ORPHA:90324 · Occasional (29-5%)
- Crigler-Najjar syndromeORPHA:205 · Occasional (29-5%)
- Hypocalcemic vitamin D-dependent ricketsORPHA:289157 · Occasional (29-5%)
- Intermediate generalized junctional epidermolysis bullosaORPHA:79402 · Occasional (29-5%)
- Lacrimoauriculodentodigital syndromeORPHA:2363 · Occasional (29-5%)
- Mosaic trisomy 7 syndromeORPHA:1747 · Occasional (29-5%)
- Naegeli-Franceschetti-Jadassohn syndromeORPHA:69087 · Occasional (29-5%)
- Nail-patella syndromeORPHA:2614 · Occasional (29-5%)
- Oculoskeletodental syndromeORPHA:557003 · Occasional (29-5%)
- OligodontiaORPHA:99798 · Occasional (29-5%)
- Orofaciodigital syndrome type 5ORPHA:2919 · Occasional (29-5%)
- PycnodysostosisORPHA:763 · Occasional (29-5%)
- TrichothiodystrophyORPHA:33364 · Occasional (29-5%)
- Sjögren-Larsson syndromeORPHA:816 · Very rare (<4-1%)
- Autosomal recessive generalized dystrophic epidermolysis bullosa, severe formORPHA:79408 · Excluded (0%)
- Localized dystrophic epidermolysis bullosa, pretibial formORPHA:79410 · Excluded (0%)
- Recessive dystrophic epidermolysis bullosa inversaORPHA:79409 · Excluded (0%)
- Self-improving dystrophic epidermolysis bullosaORPHA:79411 · Excluded (0%)